Canonical Allele Identifier: CA058824
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 406859
dbSNP Id: rs774237159

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332461C>T , CM000663.2:g.45332461C>T GRCh38
NC_000001.10:g.45798133C>T , CM000663.1:g.45798133C>T GRCh37
NC_000001.9:g.45570720C>T NCBI36
NG_008189.1:g.13010G>A , LRG_220:g.13010G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450313.6:c.644G>A ENSP00000408176.2:p.Ser215Asn
ENST00000456914.7:c.634G>A MANE Select ENSP00000407590.2:p.Ala212Thr
ENST00000461495.6:c.*373G>A ENSP00000437166.1:p.=
ENST00000671898.1:c.1222G>A ENSP00000499896.1:p.Ala408Thr
ENST00000672011.1:c.602G>A ENSP00000500418.1:p.Ser201Asn
ENST00000672314.1:c.634G>A ENSP00000500828.1:p.Ala212Thr
ENST00000672593.1:c.*607G>A ENSP00000500455.1:p.=
ENST00000672764.1:c.593G>A ENSP00000500886.1:p.Ser198Asn
ENST00000672818.2:c.709G>A ENSP00000500891.1:p.Ala237Thr
ENST00000673134.1:c.*331G>A ENSP00000500526.1:p.=
ENST00000674679.1:n.662G>A ENSP00000501623.1:p.=
ENST00000354383.10:c.637G>A ENSP00000346354.6:p.Ala213Thr
ENST00000355498.6:c.634G>A ENSP00000347685.2:p.Ala212Thr
ENST00000372098.7:c.709G>A ENSP00000361170.3:p.Ala237Thr
ENST00000372104.5:c.634G>A ENSP00000361176.1:p.Ala212Thr
ENST00000372110.7:c.679G>A ENSP00000361182.3:p.Ala227Thr
ENST00000372115.7:c.676G>A ENSP00000361187.3:p.Ala226Thr
ENST00000412971.5:c.250G>A ENSP00000410263.1:p.Ala84Thr
ENST00000435155.1:c.667G>A ENSP00000403655.1:p.Ala223Thr
ENST00000448481.5:c.667G>A ENSP00000409718.1:p.Ala223Thr
ENST00000450313.5:c.718G>A ENSP00000408176.1:p.Ala240Thr
ENST00000456914.6:c.634G>A ENSP00000407590.2:p.Ala212Thr
ENST00000461495.5:c.*373G>A ENSP00000437166.1:p.=
ENST00000462388.5:n.325G>A
ENST00000467459.5:n.28G>A ENSP00000435889.1:p.Ala10Thr
ENST00000467940.5:c.*557G>A ENSP00000436478.1:p.=
ENST00000470256.5:c.521G>A ENSP00000434985.1:p.Ser174Asn
ENST00000475516.5:c.*447G>A ENSP00000433843.1:p.=
ENST00000478796.5:n.621G>A
ENST00000481571.5:c.*447G>A ENSP00000436597.1:p.=
ENST00000488731.6:c.187+302G>A ENSP00000432330.1:p.=
ENST00000525160.5:c.*285G>A ENSP00000431568.1:p.=
ENST00000528013.6:c.676G>A ENSP00000433130.2:p.Ala226Thr
ENST00000529984.5:c.187+302G>A ENSP00000437093.1:p.=
ENST00000531105.5:c.115+1930G>A ENSP00000431292.1:p.=
ENST00000533178.5:n.263G>A ENSP00000436430.1:p.Ser88Asn
NM_001048171.1:c.676G>A NP_001041636.1:p.Ala226Thr
NM_001048172.1:c.637G>A NP_001041637.1:p.Ala213Thr
NM_001048173.1:c.634G>A NP_001041638.1:p.Ala212Thr
NM_001048174.1:c.634G>A NP_001041639.1:p.Ala212Thr
NM_001128425.1:c.718G>A , LRG_220t1:c.718G>A NP_001121897.1:p.Ala240Thr
NM_001293190.1:c.679G>A NP_001280119.1:p.Ala227Thr
NM_001293191.1:c.667G>A NP_001280120.1:p.Ala223Thr
NM_001293192.1:c.358G>A NP_001280121.1:p.Ala120Thr
NM_001293195.1:c.634G>A NP_001280124.1:p.Ala212Thr
NM_001293196.1:c.358G>A NP_001280125.1:p.Ala120Thr
NM_012222.2:c.709G>A NP_036354.1:p.Ala237Thr
XM_011541497.1:c.694G>A XP_011539799.1:p.Ala232Thr
XM_011541498.1:c.676G>A XP_011539800.1:p.Ala226Thr
XM_011541499.1:c.676G>A XP_011539801.1:p.Ala226Thr
XM_011541500.1:c.676G>A XP_011539802.1:p.Ala226Thr
XM_011541501.1:c.676G>A XP_011539803.1:p.Ala226Thr
XM_011541502.1:c.676G>A XP_011539804.1:p.Ala226Thr
XM_011541503.1:c.676G>A XP_011539805.1:p.Ala226Thr
XM_011541504.1:c.667G>A XP_011539806.1:p.Ala223Thr
XM_011541505.1:c.256G>A XP_011539807.1:p.Ala86Thr
XM_011541506.1:c.256G>A XP_011539808.1:p.Ala86Thr
XM_011541507.1:c.247G>A XP_011539809.1:p.Ala83Thr
XM_011541508.1:c.262G>A XP_011539810.1:p.Ala88Thr
XR_946658.1:n.765G>A
NM_001350650.1:c.289G>A NP_001337579.1:p.Ala97Thr
NM_001350651.1:c.289G>A NP_001337580.1:p.Ala97Thr
NR_146882.1:n.892G>A
NR_146883.1:n.706G>A
XM_011541497.3:c.694G>A XP_011539799.1:p.Ala232Thr
XM_011541500.3:c.676G>A XP_011539802.1:p.Ala226Thr
XM_011541501.2:c.676G>A XP_011539803.1:p.Ala226Thr
XM_011541502.2:c.676G>A XP_011539804.1:p.Ala226Thr
XM_011541503.2:c.676G>A XP_011539805.1:p.Ala226Thr
XM_011541504.2:c.667G>A XP_011539806.1:p.Ala223Thr
XM_011541505.2:c.256G>A XP_011539807.1:p.Ala86Thr
XM_011541506.2:c.256G>A XP_011539808.1:p.Ala86Thr
XM_017001331.1:c.676G>A XP_016856820.1:p.Ala226Thr
XM_017001332.1:c.676G>A XP_016856821.1:p.Ala226Thr
XM_017001333.1:c.676G>A XP_016856822.1:p.Ala226Thr
XM_017001334.1:c.637G>A XP_016856823.1:p.Ala213Thr
XM_017001335.1:c.358G>A XP_016856824.1:p.Ala120Thr
XM_017001336.1:c.289G>A XP_016856825.1:p.Ala97Thr
XM_017001337.1:c.289G>A XP_016856826.1:p.Ala97Thr
XM_024447244.1:c.289G>A XP_024303012.1:p.Ala97Thr
XM_024447245.1:c.289G>A XP_024303013.1:p.Ala97Thr
XM_024447248.1:c.247G>A XP_024303016.1:p.Ala83Thr
XM_024447249.1:c.118G>A XP_024303017.1:p.Ala40Thr
XM_024447250.1:c.118G>A XP_024303018.1:p.Ala40Thr
XM_024447251.1:c.118G>A XP_024303019.1:p.Ala40Thr
XR_001737190.1:n.679G>A
XR_001737192.1:n.491G>A
XR_002956643.1:n.671G>A
XR_002956644.1:n.1206G>A
XR_946658.2:n.779G>A
NM_001048171.2:c.634G>A NP_001041636.2:p.Ala212Thr
NM_001128425.2:c.718G>A NP_001121897.1:p.Ala240Thr
NM_001048172.2:c.637G>A NP_001041637.1:p.Ala213Thr
NM_001048173.2:c.634G>A NP_001041638.1:p.Ala212Thr
NM_001048174.2:c.634G>A MANE Select NP_001041639.1:p.Ala212Thr
NM_001293190.2:c.679G>A NP_001280119.1:p.Ala227Thr
NM_001293191.2:c.667G>A NP_001280120.1:p.Ala223Thr
NM_001293192.2:c.358G>A NP_001280121.1:p.Ala120Thr
NM_001293195.2:c.634G>A NP_001280124.1:p.Ala212Thr
NM_001293196.2:c.358G>A NP_001280125.1:p.Ala120Thr
NM_001350650.2:c.289G>A NP_001337579.1:p.Ala97Thr
NM_001350651.2:c.289G>A NP_001337580.1:p.Ala97Thr
NM_012222.3:c.709G>A NP_036354.1:p.Ala237Thr
NR_146882.2:n.862G>A
NR_146883.2:n.711G>A