Canonical Allele Identifier: CA15070465
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs3219472

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45338378C>T , CM000663.2:g.45338378C>T GRCh38
NC_000001.10:g.45804050C>T , CM000663.1:g.45804050C>T GRCh37
NC_000001.9:g.45576637C>T NCBI36
NG_008189.1:g.7093G>A , LRG_220:g.7093G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450313.6:c.36+1841G>A ENSP00000408176.2:p.=
ENST00000456914.7:c.-7+1521G>A MANE Select ENSP00000407590.2:p.=
ENST00000461495.6:c.36+1841G>A ENSP00000437166.1:p.=
ENST00000671856.1:n.14+1841G>A
ENST00000671898.1:c.541-3867G>A ENSP00000499896.1:p.=
ENST00000672011.1:c.36+1841G>A ENSP00000500418.1:p.=
ENST00000672593.1:c.-7+129G>A ENSP00000500455.1:p.=
ENST00000672764.1:c.-7+1598G>A ENSP00000500886.1:p.=
ENST00000672818.2:c.36+1841G>A ENSP00000500891.1:p.=
ENST00000673134.1:c.-7+1598G>A ENSP00000500526.1:p.=
ENST00000354383.10:c.-7+1598G>A ENSP00000346354.6:p.=
ENST00000355498.6:c.-7+1598G>A ENSP00000347685.2:p.=
ENST00000372098.7:c.36+1841G>A ENSP00000361170.3:p.=
ENST00000372104.5:c.-7+129G>A ENSP00000361176.1:p.=
ENST00000372110.7:c.36+1841G>A ENSP00000361182.3:p.=
ENST00000372115.7:c.36+1841G>A ENSP00000361187.3:p.=
ENST00000412971.5:c.36+1841G>A ENSP00000410263.1:p.=
ENST00000435155.1:c.-7+1598G>A ENSP00000403655.1:p.=
ENST00000448481.5:c.-7+1521G>A ENSP00000409718.1:p.=
ENST00000450313.5:c.36+1841G>A ENSP00000408176.1:p.=
ENST00000456914.6:c.-7+1521G>A ENSP00000407590.2:p.=
ENST00000461495.5:c.36+1841G>A ENSP00000437166.1:p.=
ENST00000462387.5:n.214+1841G>A
ENST00000467940.5:c.52+1825G>A ENSP00000436478.1:p.=
ENST00000470256.5:c.-7+1598G>A ENSP00000434985.1:p.=
ENST00000474703.1:n.116+1598G>A
ENST00000475516.5:c.-7+1598G>A ENSP00000433843.1:p.=
ENST00000476789.5:n.214+1841G>A
ENST00000479746.6:n.57+1521G>A
ENST00000481139.5:n.197+1841G>A
ENST00000481571.5:c.36+1841G>A ENSP00000436597.1:p.=
ENST00000483127.1:c.-181G>A ENSP00000436469.1:p.=
ENST00000483642.5:n.175+1845G>A
ENST00000485484.5:n.44+1521G>A
ENST00000488731.6:c.-7+1598G>A ENSP00000432330.1:p.=
ENST00000492494.5:n.57+1521G>A
ENST00000525160.5:c.36+1841G>A ENSP00000431568.1:p.=
ENST00000528013.6:c.-7+1521G>A ENSP00000433130.2:p.=
ENST00000529984.5:c.-7+1841G>A ENSP00000437093.1:p.=
ENST00000531105.5:c.-7+1598G>A ENSP00000431292.1:p.=
ENST00000534453.1:n.260+1598G>A
NM_001048171.1:c.36+1841G>A NP_001041636.1:p.=
NM_001048172.1:c.-7+1598G>A NP_001041637.1:p.=
NM_001048173.1:c.-7+1598G>A NP_001041638.1:p.=
NM_001048174.1:c.-7+1521G>A NP_001041639.1:p.=
NM_001128425.1:c.36+1841G>A , LRG_220t1:c.36+1841G>A NP_001121897.1:p.=
NM_001293190.1:c.36+1841G>A NP_001280119.1:p.=
NM_001293191.1:c.-7+1521G>A NP_001280120.1:p.=
NM_001293192.1:c.-219+1841G>A NP_001280121.1:p.=
NM_001293195.1:c.-7+129G>A NP_001280124.1:p.=
NM_001293196.1:c.-219+1598G>A NP_001280125.1:p.=
NM_012222.2:c.36+1841G>A NP_036354.1:p.=
XM_011541497.1:c.-181G>A XP_011539799.1:p.=
XM_011541498.1:c.-7+1598G>A XP_011539800.1:p.=
XM_011541499.1:c.-7+1521G>A XP_011539801.1:p.=
XM_011541500.1:c.-7+129G>A XP_011539802.1:p.=
XM_011541501.1:c.-7+129G>A XP_011539803.1:p.=
XM_011541502.1:c.-7+1284G>A XP_011539804.1:p.=
XM_011541503.1:c.36+1841G>A XP_011539805.1:p.=
XM_011541504.1:c.-7+1598G>A XP_011539806.1:p.=
XM_011541505.1:c.-80+1841G>A XP_011539807.1:p.=
XM_011541506.1:c.-80+1598G>A XP_011539808.1:p.=
XR_946658.1:n.83+1841G>A
NM_001350650.1:c.-278+1841G>A NP_001337579.1:p.=
NM_001350651.1:c.-214+1841G>A NP_001337580.1:p.=
NR_146882.1:n.252+1841G>A
NR_146883.1:n.140+1598G>A
XM_011541497.3:c.-181G>A XP_011539799.1:p.=
XM_011541500.3:c.-7+129G>A XP_011539802.1:p.=
XM_011541501.2:c.-7+129G>A XP_011539803.1:p.=
XM_011541502.2:c.-7+1284G>A XP_011539804.1:p.=
XM_011541503.2:c.36+1841G>A XP_011539805.1:p.=
XM_011541504.2:c.-7+1598G>A XP_011539806.1:p.=
XM_011541505.2:c.-80+1841G>A XP_011539807.1:p.=
XM_011541506.2:c.-80+1598G>A XP_011539808.1:p.=
XM_017001331.1:c.-7+1825G>A XP_016856820.1:p.=
XM_017001332.1:c.-7+1845G>A XP_016856821.1:p.=
XM_017001334.1:c.-7+1521G>A XP_016856823.1:p.=
XM_017001335.1:c.-219+1825G>A XP_016856824.1:p.=
XM_017001336.1:c.-311+1841G>A XP_016856825.1:p.=
XM_017001337.1:c.-311+1598G>A XP_016856826.1:p.=
XM_024447244.1:c.-320+1841G>A XP_024303012.1:p.=
XM_024447245.1:c.-281+1598G>A XP_024303013.1:p.=
XM_024447248.1:c.-278+1841G>A XP_024303016.1:p.=
XM_024447249.1:c.-774+1845G>A XP_024303017.1:p.=
XM_024447250.1:c.-777+1825G>A XP_024303018.1:p.=
XM_024447251.1:c.-468+1598G>A XP_024303019.1:p.=
XR_001737190.1:n.103+1841G>A
XR_001737192.1:n.31+1598G>A
XR_002956643.1:n.211+1841G>A
XR_002956644.1:n.229+1841G>A
XR_946658.2:n.97+1841G>A
NM_001048171.2:c.-7+1841G>A NP_001041636.2:p.=
NM_001128425.2:c.36+1841G>A NP_001121897.1:p.=
NM_001048172.2:c.-7+1598G>A NP_001041637.1:p.=
NM_001048173.2:c.-7+1598G>A NP_001041638.1:p.=
NM_001048174.2:c.-7+1521G>A MANE Select NP_001041639.1:p.=
NM_001293190.2:c.36+1841G>A NP_001280119.1:p.=
NM_001293191.2:c.-7+1521G>A NP_001280120.1:p.=
NM_001293192.2:c.-219+1841G>A NP_001280121.1:p.=
NM_001293195.2:c.-7+129G>A NP_001280124.1:p.=
NM_001293196.2:c.-219+1598G>A NP_001280125.1:p.=
NM_001350650.2:c.-278+1841G>A NP_001337579.1:p.=
NM_001350651.2:c.-214+1841G>A NP_001337580.1:p.=
NM_012222.3:c.36+1841G>A NP_036354.1:p.=
NR_146882.2:n.222+1841G>A
NR_146883.2:n.145+1598G>A