Canonical Allele Identifier: CA2473712120

Gene: MUTYH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331254_45331256delinsGGT , CM000663.2:g.45331254_45331256delinsGGT	GRCh38
NC_000001.10:g.45796926_45796928delinsGGT , CM000663.1:g.45796926_45796928delinsGGT	GRCh37
NC_000001.9:g.45569513_45569515delinsGGT	NCBI36
NG_008189.1:g.14215_14217delinsACC , LRG_220:g.14215_14217delinsACC

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.934_936delinsACC	ENSP00000410263.2:p.Thr312=
ENST00000435155.2:c.1351_1353delinsACC	ENSP00000403655.2:p.Thr451=
ENST00000467459.6:c.*180_*182delinsACC	ENSP00000435889.2:n.*180_*182delinsACC
ENST00000483127.2:c.1336_1338delinsACC	ENSP00000436469.2:p.Thr446=
ENST00000485271.6:c.1318_1320delinsACC	ENSP00000431264.2:p.Thr440=
ENST00000529892.6:c.1171_1173delinsACC	ENSP00000432528.2:p.Thr391=
ENST00000533178.6:c.*647_*649delinsACC	ENSP00000436430.2:n.*647_*649delinsACC
ENST00000672314.2:c.1318_1320delinsACC	ENSP00000500828.2:p.Thr440=
ENST00000710952.2:c.1402_1404delinsACC MANE Plus Clinical	ENSP00000518552.2:p.Thr468=
ENST00000672818.3:c.1393_1395delinsACC	ENSP00000500891.1:p.Thr465=
ENST00000456914.7:c.1318_1320delinsACC MANE Select	ENSP00000407590.2:p.Thr440=
ENST00000671898.1:c.1906_1908delinsACC	ENSP00000499896.1:p.Thr636=
ENST00000672011.1:c.*647_*649delinsACC	ENSP00000500418.1:n.*647_*649delinsACC
ENST00000672314.1:c.1318_1320delinsACC	ENSP00000500828.1:p.Thr440=
ENST00000672818.2:c.1393_1395delinsACC	ENSP00000500891.1:p.Thr465=
ENST00000673134.1:c.*1015_*1017delinsACC	ENSP00000500526.1:n.*1015_*1017delinsACC
ENST00000354383.10:c.1321_1323delinsACC	ENSP00000346354.6:p.Thr441=
ENST00000355498.6:c.1318_1320delinsACC	ENSP00000347685.2:p.Thr440=
ENST00000372098.7:c.1393_1395delinsACC	ENSP00000361170.3:p.Thr465=
ENST00000372104.5:c.1318_1320delinsACC	ENSP00000361176.1:p.Thr440=
ENST00000372110.7:c.1363_1365delinsACC	ENSP00000361182.3:p.Thr455=
ENST00000372115.7:c.1360_1362delinsACC	ENSP00000361187.3:p.Thr454=
ENST00000448481.5:c.1351_1353delinsACC	ENSP00000409718.1:p.Thr451=
ENST00000450313.5:c.1402_1404delinsACC	ENSP00000408176.1:p.Thr468=
ENST00000456914.6:c.1318_1320delinsACC	ENSP00000407590.2:p.Thr440=
ENST00000467459.5:c.735_737delinsACC	ENSP00000435889.1:n.735_737delinsACC
ENST00000475516.5:c.*1131_*1133delinsACC	ENSP00000433843.1:n.*1131_*1133delinsACC
ENST00000481571.5:c.*1131_*1133delinsACC	ENSP00000436597.1:n.*1131_*1133delinsACC
ENST00000482094.5:n.639_641delinsACC
ENST00000485271.5:c.15_17delinsACC
ENST00000488731.6:c.403_405delinsACC	ENSP00000432330.1:p.Thr135=
ENST00000528013.6:c.1360_1362delinsACC	ENSP00000433130.2:p.Thr454=
ENST00000529892.5:c.393_395delinsACC
ENST00000529984.5:c.403_405delinsACC	ENSP00000437093.1:p.Thr135=
ENST00000531105.5:c.116-1819_116-1817delinsACC	ENSP00000431292.1:n.116-1819_116-1817deli...
ENST00000533178.5:c.947_949delinsACC	ENSP00000436430.1:n.947_949delinsACC
NM_001048171.1:c.1360_1362delinsACC	NP_001041636.1:p.Thr454=
NM_001048172.1:c.1321_1323delinsACC	NP_001041637.1:p.Thr441=
NM_001048173.1:c.1318_1320delinsACC	NP_001041638.1:p.Thr440=
NM_001048174.1:c.1318_1320delinsACC	NP_001041639.1:p.Thr440=
NM_001128425.1:c.1402_1404delinsACC , LRG_220t1:c.1402_1404delinsACC	NP_001121897.1:p.Thr468=
NM_001293190.1:c.1363_1365delinsACC	NP_001280119.1:p.Thr455=
NM_001293191.1:c.1351_1353delinsACC	NP_001280120.1:p.Thr451=
NM_001293192.1:c.1042_1044delinsACC	NP_001280121.1:p.Thr348=
NM_001293195.1:c.1318_1320delinsACC	NP_001280124.1:p.Thr440=
NM_001293196.1:c.1042_1044delinsACC	NP_001280125.1:p.Thr348=
NM_012222.2:c.1393_1395delinsACC	NP_036354.1:p.Thr465=
XM_011541497.1:c.1378_1380delinsACC	XP_011539799.1:p.Thr460=
XM_011541498.1:c.1360_1362delinsACC	XP_011539800.1:p.Thr454=
XM_011541499.1:c.1360_1362delinsACC	XP_011539801.1:p.Thr454=
XM_011541500.1:c.1360_1362delinsACC	XP_011539802.1:p.Thr454=
XM_011541501.1:c.1360_1362delinsACC	XP_011539803.1:p.Thr454=
XM_011541502.1:c.1360_1362delinsACC	XP_011539804.1:p.Thr454=
XM_011541503.1:c.1360_1362delinsACC	XP_011539805.1:p.Thr454=
XM_011541504.1:c.1351_1353delinsACC	XP_011539806.1:p.Thr451=
XM_011541505.1:c.940_942delinsACC	XP_011539807.1:p.Thr314=
XM_011541506.1:c.940_942delinsACC	XP_011539808.1:p.Thr314=
XM_011541507.1:c.931_933delinsACC	XP_011539809.1:p.Thr311=
XM_011541508.1:c.946_948delinsACC	XP_011539810.1:p.Thr316=
XR_946658.1:n.1449_1451delinsACC
NM_001350650.1:c.973_975delinsACC	NP_001337579.1:p.Thr325=
NM_001350651.1:c.973_975delinsACC	NP_001337580.1:p.Thr325=
NR_146882.1:n.1576_1578delinsACC
NR_146883.1:n.1390_1392delinsACC
XM_011541497.3:c.1378_1380delinsACC	XP_011539799.1:p.Thr460=
XM_011541500.3:c.1360_1362delinsACC	XP_011539802.1:p.Thr454=
XM_011541501.2:c.1360_1362delinsACC	XP_011539803.1:p.Thr454=
XM_011541502.2:c.1360_1362delinsACC	XP_011539804.1:p.Thr454=
XM_011541503.2:c.1360_1362delinsACC	XP_011539805.1:p.Thr454=
XM_011541504.2:c.1351_1353delinsACC	XP_011539806.1:p.Thr451=
XM_011541505.2:c.940_942delinsACC	XP_011539807.1:p.Thr314=
XM_011541506.2:c.940_942delinsACC	XP_011539808.1:p.Thr314=
XM_017001331.1:c.1360_1362delinsACC	XP_016856820.1:p.Thr454=
XM_017001332.1:c.1360_1362delinsACC	XP_016856821.1:p.Thr454=
XM_017001333.1:c.1360_1362delinsACC	XP_016856822.1:p.Thr454=
XM_017001334.1:c.1321_1323delinsACC	XP_016856823.1:p.Thr441=
XM_017001335.1:c.1042_1044delinsACC	XP_016856824.1:p.Thr348=
XM_017001336.1:c.973_975delinsACC	XP_016856825.1:p.Thr325=
XM_017001337.1:c.973_975delinsACC	XP_016856826.1:p.Thr325=
XM_024447244.1:c.973_975delinsACC	XP_024303012.1:p.Thr325=
XM_024447245.1:c.973_975delinsACC	XP_024303013.1:p.Thr325=
XM_024447248.1:c.931_933delinsACC	XP_024303016.1:p.Thr311=
XM_024447249.1:c.802_804delinsACC	XP_024303017.1:p.Thr268=
XM_024447250.1:c.802_804delinsACC	XP_024303018.1:p.Thr268=
XM_024447251.1:c.802_804delinsACC	XP_024303019.1:p.Thr268=
XR_001737190.1:n.1363_1365delinsACC
XR_001737192.1:n.1175_1177delinsACC
XR_002956643.1:n.1355_1357delinsACC
XR_002956644.1:n.1890_1892delinsACC
XR_946658.2:n.1463_1465delinsACC
NM_001048171.2:c.1318_1320delinsACC	NP_001041636.2:p.Thr440=
NM_001128425.2:c.1402_1404delinsACC MANE Plus Clinical	NP_001121897.1:p.Thr468=
NM_001048172.2:c.1321_1323delinsACC	NP_001041637.1:p.Thr441=
NM_001048173.2:c.1318_1320delinsACC	NP_001041638.1:p.Thr440=
NM_001048174.2:c.1318_1320delinsACC MANE Select	NP_001041639.1:p.Thr440=
NM_001293190.2:c.1363_1365delinsACC	NP_001280119.1:p.Thr455=
NM_001293191.2:c.1351_1353delinsACC	NP_001280120.1:p.Thr451=
NM_001293192.2:c.1042_1044delinsACC	NP_001280121.1:p.Thr348=
NM_001293195.2:c.1318_1320delinsACC	NP_001280124.1:p.Thr440=
NM_001293196.2:c.1042_1044delinsACC	NP_001280125.1:p.Thr348=
NM_001350650.2:c.973_975delinsACC	NP_001337579.1:p.Thr325=
NM_001350651.2:c.973_975delinsACC	NP_001337580.1:p.Thr325=
NM_012222.3:c.1393_1395delinsACC	NP_036354.1:p.Thr465=
NR_146882.2:n.1546_1548delinsACC
NR_146883.2:n.1395_1397delinsACC