Canonical Allele Identifier: CA417880048
Gene: MUTYH HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45798608C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332936C>G , CM000663.2:g.45332936C>G GRCh38
NC_000001.10:g.45798608C>G , CM000663.1:g.45798608C>G GRCh37
NC_000001.9:g.45571195C>G NCBI36
NG_008189.1:g.12535G>C , LRG_220:g.12535G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.37-102G>C ENSP00000410263.2:n.37-102G>C
ENST00000435155.2:c.435G>C ENSP00000403655.2:p.Leu145=
ENST00000467459.6:c.402G>C ENSP00000435889.2:p.Leu134=
ENST00000483127.2:c.420G>C ENSP00000436469.2:p.Leu140=
ENST00000485271.6:c.402G>C ENSP00000431264.2:p.Leu134=
ENST00000529892.6:c.444G>C ENSP00000432528.2:p.Leu148=
ENST00000533178.6:c.116-249G>C ENSP00000436430.2:n.116-249G>C
ENST00000672314.2:c.402G>C ENSP00000500828.2:p.Leu134=
ENST00000674679.2:c.*314G>C ENSP00000501623.2:n.*314G>C
ENST00000710952.2:c.486G>C MANE Plus Clinical ENSP00000518552.2:p.Leu162=
ENST00000672818.3:c.477G>C ENSP00000500891.1:p.Leu159=
ENST00000450313.6:c.412G>C ENSP00000408176.2:p.Gly138Arg
ENST00000456914.7:c.402G>C MANE Select ENSP00000407590.2:p.Leu134=
ENST00000461495.6:c.*141G>C ENSP00000437166.1:n.*141G>C
ENST00000671856.1:n.348G>C
ENST00000671898.1:c.990G>C ENSP00000499896.1:p.Leu330=
ENST00000672011.1:c.370G>C ENSP00000500418.1:p.Gly124Arg
ENST00000672314.1:c.402G>C ENSP00000500828.1:p.Leu134=
ENST00000672593.1:c.*215G>C ENSP00000500455.1:n.*215G>C
ENST00000672764.1:c.361G>C ENSP00000500886.1:p.Gly121Arg
ENST00000672818.2:c.477G>C ENSP00000500891.1:p.Leu159=
ENST00000673134.1:c.*118-102G>C ENSP00000500526.1:n.*118-102G>C
ENST00000674679.1:c.430G>C ENSP00000501623.1:n.430G>C
ENST00000354383.10:c.405G>C ENSP00000346354.6:p.Leu135=
ENST00000355498.6:c.402G>C ENSP00000347685.2:p.Leu134=
ENST00000372098.7:c.477G>C ENSP00000361170.3:p.Leu159=
ENST00000372104.5:c.402G>C ENSP00000361176.1:p.Leu134=
ENST00000372110.7:c.447G>C ENSP00000361182.3:p.Leu149=
ENST00000372115.7:c.444G>C ENSP00000361187.3:p.Leu148=
ENST00000412971.5:c.37-102G>C ENSP00000410263.1:n.37-102G>C
ENST00000435155.1:c.435G>C ENSP00000403655.1:p.Leu145=
ENST00000448481.5:c.435G>C ENSP00000409718.1:p.Leu145=
ENST00000450313.5:c.486G>C ENSP00000408176.1:p.Leu162=
ENST00000456914.6:c.402G>C ENSP00000407590.2:p.Leu134=
ENST00000461495.5:c.*141G>C ENSP00000437166.1:n.*141G>C
ENST00000462387.5:n.724G>C
ENST00000462388.5:n.10G>C
ENST00000467940.5:c.*325G>C ENSP00000436478.1:n.*325G>C
ENST00000470256.5:c.308-102G>C ENSP00000434985.1:n.308-102G>C
ENST00000475516.5:c.*215G>C ENSP00000433843.1:n.*215G>C
ENST00000476789.5:n.759G>C
ENST00000478796.5:n.389G>C
ENST00000479746.6:n.602G>C
ENST00000481139.5:n.792G>C
ENST00000481571.5:c.*215G>C ENSP00000436597.1:n.*215G>C
ENST00000483642.5:n.834G>C
ENST00000485484.5:n.703G>C
ENST00000488731.6:c.116-102G>C ENSP00000432330.1:n.116-102G>C
ENST00000492494.5:n.716G>C
ENST00000525160.5:c.*53G>C ENSP00000431568.1:n.*53G>C
ENST00000528013.6:c.444G>C ENSP00000433130.2:p.Leu148=
ENST00000529984.5:c.116-102G>C ENSP00000437093.1:n.116-102G>C
ENST00000531105.5:c.115+1455G>C ENSP00000431292.1:n.115+1455G>C
ENST00000533178.5:c.122-249G>C ENSP00000436430.1:n.122-249G>C
NM_001048171.1:c.444G>C NP_001041636.1:p.Leu148=
NM_001048172.1:c.405G>C NP_001041637.1:p.Leu135=
NM_001048173.1:c.402G>C NP_001041638.1:p.Leu134=
NM_001048174.1:c.402G>C NP_001041639.1:p.Leu134=
NM_001128425.1:c.486G>C , LRG_220t1:c.486G>C NP_001121897.1:p.Leu162=
NM_001293190.1:c.447G>C NP_001280119.1:p.Leu149=
NM_001293191.1:c.435G>C NP_001280120.1:p.Leu145=
NM_001293192.1:c.126G>C NP_001280121.1:p.Leu42=
NM_001293195.1:c.402G>C NP_001280124.1:p.Leu134=
NM_001293196.1:c.126G>C NP_001280125.1:p.Leu42=
NM_012222.2:c.477G>C NP_036354.1:p.Leu159=
XM_011541497.1:c.462G>C XP_011539799.1:p.Leu154=
XM_011541498.1:c.444G>C XP_011539800.1:p.Leu148=
XM_011541499.1:c.444G>C XP_011539801.1:p.Leu148=
XM_011541500.1:c.444G>C XP_011539802.1:p.Leu148=
XM_011541501.1:c.444G>C XP_011539803.1:p.Leu148=
XM_011541502.1:c.444G>C XP_011539804.1:p.Leu148=
XM_011541503.1:c.463-102G>C XP_011539805.1:n.463-102G>C
XM_011541504.1:c.435G>C XP_011539806.1:p.Leu145=
XM_011541505.1:c.43-102G>C XP_011539807.1:n.43-102G>C
XM_011541506.1:c.43-102G>C XP_011539808.1:n.43-102G>C
XM_011541507.1:c.34-102G>C XP_011539809.1:n.34-102G>C
XM_011541508.1:c.30G>C XP_011539810.1:p.Leu10=
XR_946658.1:n.533G>C
NM_001350650.1:c.57G>C NP_001337579.1:p.Leu19=
NM_001350651.1:c.57G>C NP_001337580.1:p.Leu19=
NR_146882.1:n.660G>C
NR_146883.1:n.474G>C
XM_011541497.3:c.462G>C XP_011539799.1:p.Leu154=
XM_011541500.3:c.444G>C XP_011539802.1:p.Leu148=
XM_011541501.2:c.444G>C XP_011539803.1:p.Leu148=
XM_011541502.2:c.444G>C XP_011539804.1:p.Leu148=
XM_011541503.2:c.463-102G>C XP_011539805.1:n.463-102G>C
XM_011541504.2:c.435G>C XP_011539806.1:p.Leu145=
XM_011541505.2:c.43-102G>C XP_011539807.1:n.43-102G>C
XM_011541506.2:c.43-102G>C XP_011539808.1:n.43-102G>C
XM_017001331.1:c.444G>C XP_016856820.1:p.Leu148=
XM_017001332.1:c.444G>C XP_016856821.1:p.Leu148=
XM_017001333.1:c.444G>C XP_016856822.1:p.Leu148=
XM_017001334.1:c.405G>C XP_016856823.1:p.Leu135=
XM_017001335.1:c.126G>C XP_016856824.1:p.Leu42=
XM_017001336.1:c.57G>C XP_016856825.1:p.Leu19=
XM_017001337.1:c.57G>C XP_016856826.1:p.Leu19=
XM_024447244.1:c.57G>C XP_024303012.1:p.Leu19=
XM_024447245.1:c.57G>C XP_024303013.1:p.Leu19=
XM_024447248.1:c.34-102G>C XP_024303016.1:n.34-102G>C
XM_024447249.1:c.-115G>C XP_024303017.1:n.-115G>C
XM_024447250.1:c.-115G>C XP_024303018.1:n.-115G>C
XM_024447251.1:c.-198G>C XP_024303019.1:n.-198G>C
XR_001737190.1:n.447G>C
XR_001737192.1:n.278-102G>C
XR_002956643.1:n.458-102G>C
XR_002956644.1:n.891G>C
XR_946658.2:n.547G>C
NM_001048171.2:c.402G>C NP_001041636.2:p.Leu134=
NM_001128425.2:c.486G>C MANE Plus Clinical NP_001121897.1:p.Leu162=
NM_001048172.2:c.405G>C NP_001041637.1:p.Leu135=
NM_001048173.2:c.402G>C NP_001041638.1:p.Leu134=
NM_001048174.2:c.402G>C MANE Select NP_001041639.1:p.Leu134=
NM_001293190.2:c.447G>C NP_001280119.1:p.Leu149=
NM_001293191.2:c.435G>C NP_001280120.1:p.Leu145=
NM_001293192.2:c.126G>C NP_001280121.1:p.Leu42=
NM_001293195.2:c.402G>C NP_001280124.1:p.Leu134=
NM_001293196.2:c.126G>C NP_001280125.1:p.Leu42=
NM_001350650.2:c.57G>C NP_001337579.1:p.Leu19=
NM_001350651.2:c.57G>C NP_001337580.1:p.Leu19=
NM_012222.3:c.477G>C NP_036354.1:p.Leu159=
NR_146882.2:n.630G>C
NR_146883.2:n.479G>C