Canonical Allele Identifier: CA2473712155

Gene: MUTYH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331315_45331317delinsTGA , CM000663.2:g.45331315_45331317delinsTGA	GRCh38
NC_000001.10:g.45796987_45796989delinsTGA , CM000663.1:g.45796987_45796989delinsTGA	GRCh37
NC_000001.9:g.45569574_45569576delinsTGA	NCBI36
NG_008189.1:g.14154_14156delinsTCA , LRG_220:g.14154_14156delinsTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.873_875delinsTCA	ENSP00000410263.2:p.Ser291=
ENST00000435155.2:c.1290_1292delinsTCA	ENSP00000403655.2:p.Ser430=
ENST00000467459.6:c.*119_*121delinsTCA	ENSP00000435889.2:n.*119_*121delinsTCA
ENST00000483127.2:c.1275_1277delinsTCA	ENSP00000436469.2:p.Ser425=
ENST00000485271.6:c.1257_1259delinsTCA	ENSP00000431264.2:p.Ser419=
ENST00000529892.6:c.1110_1112delinsTCA	ENSP00000432528.2:p.Ser370=
ENST00000533178.6:c.*586_*588delinsTCA	ENSP00000436430.2:n.*586_*588delinsTCA
ENST00000672314.2:c.1257_1259delinsTCA	ENSP00000500828.2:p.Ser419=
ENST00000710952.2:c.1341_1343delinsTCA MANE Plus Clinical	ENSP00000518552.2:p.Ser447=
ENST00000672818.3:c.1332_1334delinsTCA	ENSP00000500891.1:p.Ser444=
ENST00000456914.7:c.1257_1259delinsTCA MANE Select	ENSP00000407590.2:p.Ser419=
ENST00000671898.1:c.1845_1847delinsTCA	ENSP00000499896.1:p.Ser615=
ENST00000672011.1:c.*586_*588delinsTCA	ENSP00000500418.1:n.*586_*588delinsTCA
ENST00000672314.1:c.1257_1259delinsTCA	ENSP00000500828.1:p.Ser419=
ENST00000672818.2:c.1332_1334delinsTCA	ENSP00000500891.1:p.Ser444=
ENST00000673134.1:c.*954_*956delinsTCA	ENSP00000500526.1:n.*954_*956delinsTCA
ENST00000354383.10:c.1260_1262delinsTCA	ENSP00000346354.6:p.Ser420=
ENST00000355498.6:c.1257_1259delinsTCA	ENSP00000347685.2:p.Ser419=
ENST00000372098.7:c.1332_1334delinsTCA	ENSP00000361170.3:p.Ser444=
ENST00000372104.5:c.1257_1259delinsTCA	ENSP00000361176.1:p.Ser419=
ENST00000372110.7:c.1302_1304delinsTCA	ENSP00000361182.3:p.Ser434=
ENST00000372115.7:c.1299_1301delinsTCA	ENSP00000361187.3:p.Ser433=
ENST00000448481.5:c.1290_1292delinsTCA	ENSP00000409718.1:p.Ser430=
ENST00000450313.5:c.1341_1343delinsTCA	ENSP00000408176.1:p.Ser447=
ENST00000456914.6:c.1257_1259delinsTCA	ENSP00000407590.2:p.Ser419=
ENST00000467459.5:c.674_676delinsTCA	ENSP00000435889.1:n.674_676delinsTCA
ENST00000475516.5:c.*1070_*1072delinsTCA	ENSP00000433843.1:n.*1070_*1072delinsTCA
ENST00000481571.5:c.*1070_*1072delinsTCA	ENSP00000436597.1:n.*1070_*1072delinsTCA
ENST00000482094.5:n.578_580delinsTCA
ENST00000488731.6:c.342_344delinsTCA	ENSP00000432330.1:p.Ser114=
ENST00000528013.6:c.1299_1301delinsTCA	ENSP00000433130.2:p.Ser433=
ENST00000529892.5:c.332_334delinsTCA
ENST00000529984.5:c.342_344delinsTCA	ENSP00000437093.1:p.Ser114=
ENST00000531105.5:c.116-1880_116-1878delinsTCA	ENSP00000431292.1:n.116-1880_116-1878delinsTCA
ENST00000533178.5:c.886_888delinsTCA	ENSP00000436430.1:n.886_888delinsTCA
NM_001048171.1:c.1299_1301delinsTCA	NP_001041636.1:p.Ser433=
NM_001048172.1:c.1260_1262delinsTCA	NP_001041637.1:p.Ser420=
NM_001048173.1:c.1257_1259delinsTCA	NP_001041638.1:p.Ser419=
NM_001048174.1:c.1257_1259delinsTCA	NP_001041639.1:p.Ser419=
NM_001128425.1:c.1341_1343delinsTCA , LRG_220t1:c.1341_1343delinsTCA	NP_001121897.1:p.Ser447=
NM_001293190.1:c.1302_1304delinsTCA	NP_001280119.1:p.Ser434=
NM_001293191.1:c.1290_1292delinsTCA	NP_001280120.1:p.Ser430=
NM_001293192.1:c.981_983delinsTCA	NP_001280121.1:p.Ser327=
NM_001293195.1:c.1257_1259delinsTCA	NP_001280124.1:p.Ser419=
NM_001293196.1:c.981_983delinsTCA	NP_001280125.1:p.Ser327=
NM_012222.2:c.1332_1334delinsTCA	NP_036354.1:p.Ser444=
XM_011541497.1:c.1317_1319delinsTCA	XP_011539799.1:p.Ser439=
XM_011541498.1:c.1299_1301delinsTCA	XP_011539800.1:p.Ser433=
XM_011541499.1:c.1299_1301delinsTCA	XP_011539801.1:p.Ser433=
XM_011541500.1:c.1299_1301delinsTCA	XP_011539802.1:p.Ser433=
XM_011541501.1:c.1299_1301delinsTCA	XP_011539803.1:p.Ser433=
XM_011541502.1:c.1299_1301delinsTCA	XP_011539804.1:p.Ser433=
XM_011541503.1:c.1299_1301delinsTCA	XP_011539805.1:p.Ser433=
XM_011541504.1:c.1290_1292delinsTCA	XP_011539806.1:p.Ser430=
XM_011541505.1:c.879_881delinsTCA	XP_011539807.1:p.Ser293=
XM_011541506.1:c.879_881delinsTCA	XP_011539808.1:p.Ser293=
XM_011541507.1:c.870_872delinsTCA	XP_011539809.1:p.Ser290=
XM_011541508.1:c.885_887delinsTCA	XP_011539810.1:p.Ser295=
XR_946658.1:n.1388_1390delinsTCA
NM_001350650.1:c.912_914delinsTCA	NP_001337579.1:p.Ser304=
NM_001350651.1:c.912_914delinsTCA	NP_001337580.1:p.Ser304=
NR_146882.1:n.1515_1517delinsTCA
NR_146883.1:n.1329_1331delinsTCA
XM_011541497.3:c.1317_1319delinsTCA	XP_011539799.1:p.Ser439=
XM_011541500.3:c.1299_1301delinsTCA	XP_011539802.1:p.Ser433=
XM_011541501.2:c.1299_1301delinsTCA	XP_011539803.1:p.Ser433=
XM_011541502.2:c.1299_1301delinsTCA	XP_011539804.1:p.Ser433=
XM_011541503.2:c.1299_1301delinsTCA	XP_011539805.1:p.Ser433=
XM_011541504.2:c.1290_1292delinsTCA	XP_011539806.1:p.Ser430=
XM_011541505.2:c.879_881delinsTCA	XP_011539807.1:p.Ser293=
XM_011541506.2:c.879_881delinsTCA	XP_011539808.1:p.Ser293=
XM_017001331.1:c.1299_1301delinsTCA	XP_016856820.1:p.Ser433=
XM_017001332.1:c.1299_1301delinsTCA	XP_016856821.1:p.Ser433=
XM_017001333.1:c.1299_1301delinsTCA	XP_016856822.1:p.Ser433=
XM_017001334.1:c.1260_1262delinsTCA	XP_016856823.1:p.Ser420=
XM_017001335.1:c.981_983delinsTCA	XP_016856824.1:p.Ser327=
XM_017001336.1:c.912_914delinsTCA	XP_016856825.1:p.Ser304=
XM_017001337.1:c.912_914delinsTCA	XP_016856826.1:p.Ser304=
XM_024447244.1:c.912_914delinsTCA	XP_024303012.1:p.Ser304=
XM_024447245.1:c.912_914delinsTCA	XP_024303013.1:p.Ser304=
XM_024447248.1:c.870_872delinsTCA	XP_024303016.1:p.Ser290=
XM_024447249.1:c.741_743delinsTCA	XP_024303017.1:p.Ser247=
XM_024447250.1:c.741_743delinsTCA	XP_024303018.1:p.Ser247=
XM_024447251.1:c.741_743delinsTCA	XP_024303019.1:p.Ser247=
XR_001737190.1:n.1302_1304delinsTCA
XR_001737192.1:n.1114_1116delinsTCA
XR_002956643.1:n.1294_1296delinsTCA
XR_002956644.1:n.1829_1831delinsTCA
XR_946658.2:n.1402_1404delinsTCA
NM_001048171.2:c.1257_1259delinsTCA	NP_001041636.2:p.Ser419=
NM_001128425.2:c.1341_1343delinsTCA MANE Plus Clinical	NP_001121897.1:p.Ser447=
NM_001048172.2:c.1260_1262delinsTCA	NP_001041637.1:p.Ser420=
NM_001048173.2:c.1257_1259delinsTCA	NP_001041638.1:p.Ser419=
NM_001048174.2:c.1257_1259delinsTCA MANE Select	NP_001041639.1:p.Ser419=
NM_001293190.2:c.1302_1304delinsTCA	NP_001280119.1:p.Ser434=
NM_001293191.2:c.1290_1292delinsTCA	NP_001280120.1:p.Ser430=
NM_001293192.2:c.981_983delinsTCA	NP_001280121.1:p.Ser327=
NM_001293195.2:c.1257_1259delinsTCA	NP_001280124.1:p.Ser419=
NM_001293196.2:c.981_983delinsTCA	NP_001280125.1:p.Ser327=
NM_001350650.2:c.912_914delinsTCA	NP_001337579.1:p.Ser304=
NM_001350651.2:c.912_914delinsTCA	NP_001337580.1:p.Ser304=
NM_012222.3:c.1332_1334delinsTCA	NP_036354.1:p.Ser444=
NR_146882.2:n.1485_1487delinsTCA
NR_146883.2:n.1334_1336delinsTCA