Canonical Allele Identifier: CA1143420531
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332446G= , CM000663.2:g.45332446G= GRCh38
NC_000001.10:g.45798118G= , CM000663.1:g.45798118G= GRCh37
NC_000001.9:g.45570705G= NCBI36
NG_008189.1:g.13025C= , LRG_220:g.13025C=

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.265C= ENSP00000410263.2:p.Arg89=
ENST00000435155.2:c.682C= ENSP00000403655.2:p.Arg228=
ENST00000467459.6:c.649C= ENSP00000435889.2:p.Arg217=
ENST00000483127.2:c.667C= ENSP00000436469.2:p.Arg223=
ENST00000485271.6:c.649C= ENSP00000431264.2:p.Arg217=
ENST00000529892.6:c.691C= ENSP00000432528.2:p.Arg231=
ENST00000533178.6:c.272C= ENSP00000436430.2:p.Pro91=
ENST00000672314.2:c.649C= ENSP00000500828.2:p.Arg217=
ENST00000674679.2:c.*561C= ENSP00000501623.2:n.*561C=
ENST00000710952.2:c.733C= MANE Plus Clinical ENSP00000518552.2:p.Arg245=
ENST00000672818.3:c.724C= ENSP00000500891.1:p.Arg242=
ENST00000450313.6:c.659C= ENSP00000408176.2:p.Pro220=
ENST00000456914.7:c.649C= MANE Select ENSP00000407590.2:p.Arg217=
ENST00000461495.6:c.*388C= ENSP00000437166.1:n.*388C=
ENST00000671898.1:c.1237C= ENSP00000499896.1:p.Arg413=
ENST00000672011.1:c.617C= ENSP00000500418.1:p.Pro206=
ENST00000672314.1:c.649C= ENSP00000500828.1:p.Arg217=
ENST00000672593.1:c.*622C= ENSP00000500455.1:n.*622C=
ENST00000672764.1:c.608C= ENSP00000500886.1:p.Pro203=
ENST00000672818.2:c.724C= ENSP00000500891.1:p.Arg242=
ENST00000673134.1:c.*346C= ENSP00000500526.1:n.*346C=
ENST00000674679.1:c.677C= ENSP00000501623.1:n.677C=
ENST00000354383.10:c.652C= ENSP00000346354.6:p.Arg218=
ENST00000355498.6:c.649C= ENSP00000347685.2:p.Arg217=
ENST00000372098.7:c.724C= ENSP00000361170.3:p.Arg242=
ENST00000372104.5:c.649C= ENSP00000361176.1:p.Arg217=
ENST00000372110.7:c.694C= ENSP00000361182.3:p.Arg232=
ENST00000372115.7:c.691C= ENSP00000361187.3:p.Arg231=
ENST00000412971.5:c.265C= ENSP00000410263.1:p.Arg89=
ENST00000435155.1:c.682C= ENSP00000403655.1:p.Arg228=
ENST00000448481.5:c.682C= ENSP00000409718.1:p.Arg228=
ENST00000450313.5:c.733C= ENSP00000408176.1:p.Arg245=
ENST00000456914.6:c.649C= ENSP00000407590.2:p.Arg217=
ENST00000461495.5:c.*388C= ENSP00000437166.1:n.*388C=
ENST00000462388.5:n.340C=
ENST00000467459.5:c.43C= ENSP00000435889.1:p.Arg15=
ENST00000467940.5:c.*572C= ENSP00000436478.1:n.*572C=
ENST00000470256.5:c.536C= ENSP00000434985.1:p.Pro179=
ENST00000475516.5:c.*462C= ENSP00000433843.1:n.*462C=
ENST00000478796.5:n.636C=
ENST00000481571.5:c.*462C= ENSP00000436597.1:n.*462C=
ENST00000488731.6:c.187+317C= ENSP00000432330.1:n.187+317C=
ENST00000525160.5:c.*300C= ENSP00000431568.1:n.*300C=
ENST00000528013.6:c.691C= ENSP00000433130.2:p.Arg231=
ENST00000529984.5:c.187+317C= ENSP00000437093.1:n.187+317C=
ENST00000531105.5:c.115+1945C= ENSP00000431292.1:n.115+1945C=
ENST00000533178.5:c.278C= ENSP00000436430.1:p.Pro93=
NM_001048171.1:c.691C= NP_001041636.1:p.Arg231=
NM_001048172.1:c.652C= NP_001041637.1:p.Arg218=
NM_001048173.1:c.649C= NP_001041638.1:p.Arg217=
NM_001048174.1:c.649C= NP_001041639.1:p.Arg217=
NM_001128425.1:c.733C= , LRG_220t1:c.733C= NP_001121897.1:p.Arg245=
NM_001293190.1:c.694C= NP_001280119.1:p.Arg232=
NM_001293191.1:c.682C= NP_001280120.1:p.Arg228=
NM_001293192.1:c.373C= NP_001280121.1:p.Arg125=
NM_001293195.1:c.649C= NP_001280124.1:p.Arg217=
NM_001293196.1:c.373C= NP_001280125.1:p.Arg125=
NM_012222.2:c.724C= NP_036354.1:p.Arg242=
XM_011541497.1:c.709C= XP_011539799.1:p.Arg237=
XM_011541498.1:c.691C= XP_011539800.1:p.Arg231=
XM_011541499.1:c.691C= XP_011539801.1:p.Arg231=
XM_011541500.1:c.691C= XP_011539802.1:p.Arg231=
XM_011541501.1:c.691C= XP_011539803.1:p.Arg231=
XM_011541502.1:c.691C= XP_011539804.1:p.Arg231=
XM_011541503.1:c.691C= XP_011539805.1:p.Arg231=
XM_011541504.1:c.682C= XP_011539806.1:p.Arg228=
XM_011541505.1:c.271C= XP_011539807.1:p.Arg91=
XM_011541506.1:c.271C= XP_011539808.1:p.Arg91=
XM_011541507.1:c.262C= XP_011539809.1:p.Arg88=
XM_011541508.1:c.277C= XP_011539810.1:p.Arg93=
XR_946658.1:n.780C=
NM_001350650.1:c.304C= NP_001337579.1:p.Arg102=
NM_001350651.1:c.304C= NP_001337580.1:p.Arg102=
NR_146882.1:n.907C=
NR_146883.1:n.721C=
XM_011541497.3:c.709C= XP_011539799.1:p.Arg237=
XM_011541500.3:c.691C= XP_011539802.1:p.Arg231=
XM_011541501.2:c.691C= XP_011539803.1:p.Arg231=
XM_011541502.2:c.691C= XP_011539804.1:p.Arg231=
XM_011541503.2:c.691C= XP_011539805.1:p.Arg231=
XM_011541504.2:c.682C= XP_011539806.1:p.Arg228=
XM_011541505.2:c.271C= XP_011539807.1:p.Arg91=
XM_011541506.2:c.271C= XP_011539808.1:p.Arg91=
XM_017001331.1:c.691C= XP_016856820.1:p.Arg231=
XM_017001332.1:c.691C= XP_016856821.1:p.Arg231=
XM_017001333.1:c.691C= XP_016856822.1:p.Arg231=
XM_017001334.1:c.652C= XP_016856823.1:p.Arg218=
XM_017001335.1:c.373C= XP_016856824.1:p.Arg125=
XM_017001336.1:c.304C= XP_016856825.1:p.Arg102=
XM_017001337.1:c.304C= XP_016856826.1:p.Arg102=
XM_024447244.1:c.304C= XP_024303012.1:p.Arg102=
XM_024447245.1:c.304C= XP_024303013.1:p.Arg102=
XM_024447248.1:c.262C= XP_024303016.1:p.Arg88=
XM_024447249.1:c.133C= XP_024303017.1:p.Arg45=
XM_024447250.1:c.133C= XP_024303018.1:p.Arg45=
XM_024447251.1:c.133C= XP_024303019.1:p.Arg45=
XR_001737190.1:n.694C=
XR_001737192.1:n.506C=
XR_002956643.1:n.686C=
XR_002956644.1:n.1221C=
XR_946658.2:n.794C=
NM_001048171.2:c.649C= NP_001041636.2:p.Arg217=
NM_001128425.2:c.733C= MANE Plus Clinical NP_001121897.1:p.Arg245=
NM_001048172.2:c.652C= NP_001041637.1:p.Arg218=
NM_001048173.2:c.649C= NP_001041638.1:p.Arg217=
NM_001048174.2:c.649C= MANE Select NP_001041639.1:p.Arg217=
NM_001293190.2:c.694C= NP_001280119.1:p.Arg232=
NM_001293191.2:c.682C= NP_001280120.1:p.Arg228=
NM_001293192.2:c.373C= NP_001280121.1:p.Arg125=
NM_001293195.2:c.649C= NP_001280124.1:p.Arg217=
NM_001293196.2:c.373C= NP_001280125.1:p.Arg125=
NM_001350650.2:c.304C= NP_001337579.1:p.Arg102=
NM_001350651.2:c.304C= NP_001337580.1:p.Arg102=
NM_012222.3:c.724C= NP_036354.1:p.Arg242=
NR_146882.2:n.877C=
NR_146883.2:n.726C=