Canonical Allele Identifier: CA2473712147
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331301_45331302delinsAT , CM000663.2:g.45331301_45331302delinsAT GRCh38
NC_000001.10:g.45796973_45796974delinsAT , CM000663.1:g.45796973_45796974delinsAT GRCh37
NC_000001.9:g.45569560_45569561delinsAT NCBI36
NG_008189.1:g.14169_14170delinsAT , LRG_220:g.14169_14170delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.888_889delinsAT ENSP00000410263.2:p.Thr296=
ENST00000435155.2:c.1305_1306delinsAT ENSP00000403655.2:p.Thr435=
ENST00000467459.6:c.*134_*135delinsAT ENSP00000435889.2:n.*134_*135delinsAT
ENST00000483127.2:c.1290_1291delinsAT ENSP00000436469.2:p.Thr430=
ENST00000485271.6:c.1272_1273delinsAT ENSP00000431264.2:p.Thr424=
ENST00000529892.6:c.1125_1126delinsAT ENSP00000432528.2:p.Thr375=
ENST00000533178.6:c.*601_*602delinsAT ENSP00000436430.2:n.*601_*602delinsAT
ENST00000672314.2:c.1272_1273delinsAT ENSP00000500828.2:p.Thr424=
ENST00000710952.2:c.1356_1357delinsAT MANE Plus Clinical ENSP00000518552.2:p.Thr452=
ENST00000672818.3:c.1347_1348delinsAT ENSP00000500891.1:p.Thr449=
ENST00000456914.7:c.1272_1273delinsAT MANE Select ENSP00000407590.2:p.Thr424=
ENST00000671898.1:c.1860_1861delinsAT ENSP00000499896.1:p.Thr620=
ENST00000672011.1:c.*601_*602delinsAT ENSP00000500418.1:n.*601_*602delinsAT
ENST00000672314.1:c.1272_1273delinsAT ENSP00000500828.1:p.Thr424=
ENST00000672818.2:c.1347_1348delinsAT ENSP00000500891.1:p.Thr449=
ENST00000673134.1:c.*969_*970delinsAT ENSP00000500526.1:n.*969_*970delinsAT
ENST00000354383.10:c.1275_1276delinsAT ENSP00000346354.6:p.Thr425=
ENST00000355498.6:c.1272_1273delinsAT ENSP00000347685.2:p.Thr424=
ENST00000372098.7:c.1347_1348delinsAT ENSP00000361170.3:p.Thr449=
ENST00000372104.5:c.1272_1273delinsAT ENSP00000361176.1:p.Thr424=
ENST00000372110.7:c.1317_1318delinsAT ENSP00000361182.3:p.Thr439=
ENST00000372115.7:c.1314_1315delinsAT ENSP00000361187.3:p.Thr438=
ENST00000448481.5:c.1305_1306delinsAT ENSP00000409718.1:p.Thr435=
ENST00000450313.5:c.1356_1357delinsAT ENSP00000408176.1:p.Thr452=
ENST00000456914.6:c.1272_1273delinsAT ENSP00000407590.2:p.Thr424=
ENST00000467459.5:c.689_690delinsAT ENSP00000435889.1:n.689_690delinsAT
ENST00000475516.5:c.*1085_*1086delinsAT ENSP00000433843.1:n.*1085_*1086delinsAT
ENST00000481571.5:c.*1085_*1086delinsAT ENSP00000436597.1:n.*1085_*1086delinsAT
ENST00000482094.5:n.593_594delinsAT
ENST00000488731.6:c.357_358delinsAT ENSP00000432330.1:p.Thr119=
ENST00000528013.6:c.1314_1315delinsAT ENSP00000433130.2:p.Thr438=
ENST00000529892.5:c.347_348delinsAT
ENST00000529984.5:c.357_358delinsAT ENSP00000437093.1:p.Thr119=
ENST00000531105.5:c.116-1865_116-1864delinsAT ENSP00000431292.1:n.116-1865_116-1864delinsAT
ENST00000533178.5:c.901_902delinsAT ENSP00000436430.1:n.901_902delinsAT
NM_001048171.1:c.1314_1315delinsAT NP_001041636.1:p.Thr438=
NM_001048172.1:c.1275_1276delinsAT NP_001041637.1:p.Thr425=
NM_001048173.1:c.1272_1273delinsAT NP_001041638.1:p.Thr424=
NM_001048174.1:c.1272_1273delinsAT NP_001041639.1:p.Thr424=
NM_001128425.1:c.1356_1357delinsAT , LRG_220t1:c.1356_1357delinsAT NP_001121897.1:p.Thr452=
NM_001293190.1:c.1317_1318delinsAT NP_001280119.1:p.Thr439=
NM_001293191.1:c.1305_1306delinsAT NP_001280120.1:p.Thr435=
NM_001293192.1:c.996_997delinsAT NP_001280121.1:p.Thr332=
NM_001293195.1:c.1272_1273delinsAT NP_001280124.1:p.Thr424=
NM_001293196.1:c.996_997delinsAT NP_001280125.1:p.Thr332=
NM_012222.2:c.1347_1348delinsAT NP_036354.1:p.Thr449=
XM_011541497.1:c.1332_1333delinsAT XP_011539799.1:p.Thr444=
XM_011541498.1:c.1314_1315delinsAT XP_011539800.1:p.Thr438=
XM_011541499.1:c.1314_1315delinsAT XP_011539801.1:p.Thr438=
XM_011541500.1:c.1314_1315delinsAT XP_011539802.1:p.Thr438=
XM_011541501.1:c.1314_1315delinsAT XP_011539803.1:p.Thr438=
XM_011541502.1:c.1314_1315delinsAT XP_011539804.1:p.Thr438=
XM_011541503.1:c.1314_1315delinsAT XP_011539805.1:p.Thr438=
XM_011541504.1:c.1305_1306delinsAT XP_011539806.1:p.Thr435=
XM_011541505.1:c.894_895delinsAT XP_011539807.1:p.Thr298=
XM_011541506.1:c.894_895delinsAT XP_011539808.1:p.Thr298=
XM_011541507.1:c.885_886delinsAT XP_011539809.1:p.Thr295=
XM_011541508.1:c.900_901delinsAT XP_011539810.1:p.Thr300=
XR_946658.1:n.1403_1404delinsAT
NM_001350650.1:c.927_928delinsAT NP_001337579.1:p.Thr309=
NM_001350651.1:c.927_928delinsAT NP_001337580.1:p.Thr309=
NR_146882.1:n.1530_1531delinsAT
NR_146883.1:n.1344_1345delinsAT
XM_011541497.3:c.1332_1333delinsAT XP_011539799.1:p.Thr444=
XM_011541500.3:c.1314_1315delinsAT XP_011539802.1:p.Thr438=
XM_011541501.2:c.1314_1315delinsAT XP_011539803.1:p.Thr438=
XM_011541502.2:c.1314_1315delinsAT XP_011539804.1:p.Thr438=
XM_011541503.2:c.1314_1315delinsAT XP_011539805.1:p.Thr438=
XM_011541504.2:c.1305_1306delinsAT XP_011539806.1:p.Thr435=
XM_011541505.2:c.894_895delinsAT XP_011539807.1:p.Thr298=
XM_011541506.2:c.894_895delinsAT XP_011539808.1:p.Thr298=
XM_017001331.1:c.1314_1315delinsAT XP_016856820.1:p.Thr438=
XM_017001332.1:c.1314_1315delinsAT XP_016856821.1:p.Thr438=
XM_017001333.1:c.1314_1315delinsAT XP_016856822.1:p.Thr438=
XM_017001334.1:c.1275_1276delinsAT XP_016856823.1:p.Thr425=
XM_017001335.1:c.996_997delinsAT XP_016856824.1:p.Thr332=
XM_017001336.1:c.927_928delinsAT XP_016856825.1:p.Thr309=
XM_017001337.1:c.927_928delinsAT XP_016856826.1:p.Thr309=
XM_024447244.1:c.927_928delinsAT XP_024303012.1:p.Thr309=
XM_024447245.1:c.927_928delinsAT XP_024303013.1:p.Thr309=
XM_024447248.1:c.885_886delinsAT XP_024303016.1:p.Thr295=
XM_024447249.1:c.756_757delinsAT XP_024303017.1:p.Thr252=
XM_024447250.1:c.756_757delinsAT XP_024303018.1:p.Thr252=
XM_024447251.1:c.756_757delinsAT XP_024303019.1:p.Thr252=
XR_001737190.1:n.1317_1318delinsAT
XR_001737192.1:n.1129_1130delinsAT
XR_002956643.1:n.1309_1310delinsAT
XR_002956644.1:n.1844_1845delinsAT
XR_946658.2:n.1417_1418delinsAT
NM_001048171.2:c.1272_1273delinsAT NP_001041636.2:p.Thr424=
NM_001128425.2:c.1356_1357delinsAT MANE Plus Clinical NP_001121897.1:p.Thr452=
NM_001048172.2:c.1275_1276delinsAT NP_001041637.1:p.Thr425=
NM_001048173.2:c.1272_1273delinsAT NP_001041638.1:p.Thr424=
NM_001048174.2:c.1272_1273delinsAT MANE Select NP_001041639.1:p.Thr424=
NM_001293190.2:c.1317_1318delinsAT NP_001280119.1:p.Thr439=
NM_001293191.2:c.1305_1306delinsAT NP_001280120.1:p.Thr435=
NM_001293192.2:c.996_997delinsAT NP_001280121.1:p.Thr332=
NM_001293195.2:c.1272_1273delinsAT NP_001280124.1:p.Thr424=
NM_001293196.2:c.996_997delinsAT NP_001280125.1:p.Thr332=
NM_001350650.2:c.927_928delinsAT NP_001337579.1:p.Thr309=
NM_001350651.2:c.927_928delinsAT NP_001337580.1:p.Thr309=
NM_012222.3:c.1347_1348delinsAT NP_036354.1:p.Thr449=
NR_146882.2:n.1500_1501delinsAT
NR_146883.2:n.1349_1350delinsAT