Canonical Allele Identifier: CA10577725

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 233912
• ClinVar RCV Id: RCV000219744
• dbSNP Id: rs876660729
• MyVariant Identifiers: chr1:g.45798143A>T (hg19) ; chr1:g.45332471A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332471A>T , CM000663.2:g.45332471A>T	GRCh38
NC_000001.10:g.45798143A>T , CM000663.1:g.45798143A>T	GRCh37
NC_000001.9:g.45570730A>T	NCBI36
NG_008189.1:g.13000T>A , LRG_220:g.13000T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.240T>A	ENSP00000410263.2:p.Asp80Glu
ENST00000435155.2:c.657T>A	ENSP00000403655.2:p.Asp219Glu
ENST00000467459.6:c.624T>A	ENSP00000435889.2:p.Asp208Glu
ENST00000483127.2:c.642T>A	ENSP00000436469.2:p.Asp214Glu
ENST00000485271.6:c.624T>A	ENSP00000431264.2:p.Asp208Glu
ENST00000529892.6:c.666T>A	ENSP00000432528.2:p.Asp222Glu
ENST00000533178.6:c.247T>A	ENSP00000436430.2:p.Trp83Arg
ENST00000672314.2:c.624T>A	ENSP00000500828.2:p.Asp208Glu
ENST00000674679.2:c.*536T>A	ENSP00000501623.2:n.*536T>A
ENST00000710952.2:c.708T>A MANE Plus Clinical	ENSP00000518552.2:p.Asp236Glu
ENST00000672818.3:c.699T>A	ENSP00000500891.1:p.Asp233Glu
ENST00000450313.6:c.634T>A	ENSP00000408176.2:p.Trp212Arg
ENST00000456914.7:c.624T>A MANE Select	ENSP00000407590.2:p.Asp208Glu
ENST00000461495.6:c.*363T>A	ENSP00000437166.1:n.*363T>A
ENST00000671898.1:c.1212T>A	ENSP00000499896.1:p.Asp404Glu
ENST00000672011.1:c.592T>A	ENSP00000500418.1:p.Trp198Arg
ENST00000672314.1:c.624T>A	ENSP00000500828.1:p.Asp208Glu
ENST00000672593.1:c.*597T>A	ENSP00000500455.1:n.*597T>A
ENST00000672764.1:c.583T>A	ENSP00000500886.1:p.Trp195Arg
ENST00000672818.2:c.699T>A	ENSP00000500891.1:p.Asp233Glu
ENST00000673134.1:c.*321T>A	ENSP00000500526.1:n.*321T>A
ENST00000674679.1:c.652T>A	ENSP00000501623.1:n.652T>A
ENST00000354383.10:c.627T>A	ENSP00000346354.6:p.Asp209Glu
ENST00000355498.6:c.624T>A	ENSP00000347685.2:p.Asp208Glu
ENST00000372098.7:c.699T>A	ENSP00000361170.3:p.Asp233Glu
ENST00000372104.5:c.624T>A	ENSP00000361176.1:p.Asp208Glu
ENST00000372110.7:c.669T>A	ENSP00000361182.3:p.Asp223Glu
ENST00000372115.7:c.666T>A	ENSP00000361187.3:p.Asp222Glu
ENST00000412971.5:c.240T>A	ENSP00000410263.1:p.Asp80Glu
ENST00000435155.1:c.657T>A	ENSP00000403655.1:p.Asp219Glu
ENST00000448481.5:c.657T>A	ENSP00000409718.1:p.Asp219Glu
ENST00000450313.5:c.708T>A	ENSP00000408176.1:p.Asp236Glu
ENST00000456914.6:c.624T>A	ENSP00000407590.2:p.Asp208Glu
ENST00000461495.5:c.*363T>A	ENSP00000437166.1:n.*363T>A
ENST00000462388.5:n.315T>A
ENST00000467459.5:c.18T>A	ENSP00000435889.1:p.Asp6Glu
ENST00000467940.5:c.*547T>A	ENSP00000436478.1:n.*547T>A
ENST00000470256.5:c.511T>A	ENSP00000434985.1:p.Trp171Arg
ENST00000475516.5:c.*437T>A	ENSP00000433843.1:n.*437T>A
ENST00000478796.5:n.611T>A
ENST00000481571.5:c.*437T>A	ENSP00000436597.1:n.*437T>A
ENST00000488731.6:c.187+292T>A	ENSP00000432330.1:n.187+292T>A
ENST00000525160.5:c.*275T>A	ENSP00000431568.1:n.*275T>A
ENST00000528013.6:c.666T>A	ENSP00000433130.2:p.Asp222Glu
ENST00000529984.5:c.187+292T>A	ENSP00000437093.1:n.187+292T>A
ENST00000531105.5:c.115+1920T>A	ENSP00000431292.1:n.115+1920T>A
ENST00000533178.5:c.253T>A	ENSP00000436430.1:p.Trp85Arg
NM_001048171.1:c.666T>A	NP_001041636.1:p.Asp222Glu
NM_001048172.1:c.627T>A	NP_001041637.1:p.Asp209Glu
NM_001048173.1:c.624T>A	NP_001041638.1:p.Asp208Glu
NM_001048174.1:c.624T>A	NP_001041639.1:p.Asp208Glu
NM_001128425.1:c.708T>A , LRG_220t1:c.708T>A	NP_001121897.1:p.Asp236Glu
NM_001293190.1:c.669T>A	NP_001280119.1:p.Asp223Glu
NM_001293191.1:c.657T>A	NP_001280120.1:p.Asp219Glu
NM_001293192.1:c.348T>A	NP_001280121.1:p.Asp116Glu
NM_001293195.1:c.624T>A	NP_001280124.1:p.Asp208Glu
NM_001293196.1:c.348T>A	NP_001280125.1:p.Asp116Glu
NM_012222.2:c.699T>A	NP_036354.1:p.Asp233Glu
XM_011541497.1:c.684T>A	XP_011539799.1:p.Asp228Glu
XM_011541498.1:c.666T>A	XP_011539800.1:p.Asp222Glu
XM_011541499.1:c.666T>A	XP_011539801.1:p.Asp222Glu
XM_011541500.1:c.666T>A	XP_011539802.1:p.Asp222Glu
XM_011541501.1:c.666T>A	XP_011539803.1:p.Asp222Glu
XM_011541502.1:c.666T>A	XP_011539804.1:p.Asp222Glu
XM_011541503.1:c.666T>A	XP_011539805.1:p.Asp222Glu
XM_011541504.1:c.657T>A	XP_011539806.1:p.Asp219Glu
XM_011541505.1:c.246T>A	XP_011539807.1:p.Asp82Glu
XM_011541506.1:c.246T>A	XP_011539808.1:p.Asp82Glu
XM_011541507.1:c.237T>A	XP_011539809.1:p.Asp79Glu
XM_011541508.1:c.252T>A	XP_011539810.1:p.Asp84Glu
XR_946658.1:n.755T>A
NM_001350650.1:c.279T>A	NP_001337579.1:p.Asp93Glu
NM_001350651.1:c.279T>A	NP_001337580.1:p.Asp93Glu
NR_146882.1:n.882T>A
NR_146883.1:n.696T>A
XM_011541497.3:c.684T>A	XP_011539799.1:p.Asp228Glu
XM_011541500.3:c.666T>A	XP_011539802.1:p.Asp222Glu
XM_011541501.2:c.666T>A	XP_011539803.1:p.Asp222Glu
XM_011541502.2:c.666T>A	XP_011539804.1:p.Asp222Glu
XM_011541503.2:c.666T>A	XP_011539805.1:p.Asp222Glu
XM_011541504.2:c.657T>A	XP_011539806.1:p.Asp219Glu
XM_011541505.2:c.246T>A	XP_011539807.1:p.Asp82Glu
XM_011541506.2:c.246T>A	XP_011539808.1:p.Asp82Glu
XM_017001331.1:c.666T>A	XP_016856820.1:p.Asp222Glu
XM_017001332.1:c.666T>A	XP_016856821.1:p.Asp222Glu
XM_017001333.1:c.666T>A	XP_016856822.1:p.Asp222Glu
XM_017001334.1:c.627T>A	XP_016856823.1:p.Asp209Glu
XM_017001335.1:c.348T>A	XP_016856824.1:p.Asp116Glu
XM_017001336.1:c.279T>A	XP_016856825.1:p.Asp93Glu
XM_017001337.1:c.279T>A	XP_016856826.1:p.Asp93Glu
XM_024447244.1:c.279T>A	XP_024303012.1:p.Asp93Glu
XM_024447245.1:c.279T>A	XP_024303013.1:p.Asp93Glu
XM_024447248.1:c.237T>A	XP_024303016.1:p.Asp79Glu
XM_024447249.1:c.108T>A	XP_024303017.1:p.Asp36Glu
XM_024447250.1:c.108T>A	XP_024303018.1:p.Asp36Glu
XM_024447251.1:c.108T>A	XP_024303019.1:p.Asp36Glu
XR_001737190.1:n.669T>A
XR_001737192.1:n.481T>A
XR_002956643.1:n.661T>A
XR_002956644.1:n.1196T>A
XR_946658.2:n.769T>A
NM_001048171.2:c.624T>A	NP_001041636.2:p.Asp208Glu
NM_001128425.2:c.708T>A MANE Plus Clinical	NP_001121897.1:p.Asp236Glu
NM_001048172.2:c.627T>A	NP_001041637.1:p.Asp209Glu
NM_001048173.2:c.624T>A	NP_001041638.1:p.Asp208Glu
NM_001048174.2:c.624T>A MANE Select	NP_001041639.1:p.Asp208Glu
NM_001293190.2:c.669T>A	NP_001280119.1:p.Asp223Glu
NM_001293191.2:c.657T>A	NP_001280120.1:p.Asp219Glu
NM_001293192.2:c.348T>A	NP_001280121.1:p.Asp116Glu
NM_001293195.2:c.624T>A	NP_001280124.1:p.Asp208Glu
NM_001293196.2:c.348T>A	NP_001280125.1:p.Asp116Glu
NM_001350650.2:c.279T>A	NP_001337579.1:p.Asp93Glu
NM_001350651.2:c.279T>A	NP_001337580.1:p.Asp93Glu
NM_012222.3:c.699T>A	NP_036354.1:p.Asp233Glu
NR_146882.2:n.852T>A
NR_146883.2:n.701T>A