Canonical Allele Identifier: CA340135395

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45798320C>G (hg19) ; chr1:g.45332648C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332648C>G , CM000663.2:g.45332648C>G	GRCh38
NC_000001.10:g.45798320C>G , CM000663.1:g.45798320C>G	GRCh37
NC_000001.9:g.45570907C>G	NCBI36
NG_008189.1:g.12823G>C , LRG_220:g.12823G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.148G>C	ENSP00000410263.2:p.Glu50Gln
ENST00000435155.2:c.565G>C	ENSP00000403655.2:p.Glu189Gln
ENST00000467459.6:c.532G>C	ENSP00000435889.2:p.Glu178Gln
ENST00000483127.2:c.550G>C	ENSP00000436469.2:p.Glu184Gln
ENST00000485271.6:c.532G>C	ENSP00000431264.2:p.Glu178Gln
ENST00000529892.6:c.574G>C	ENSP00000432528.2:p.Glu192Gln
ENST00000533178.6:c.155G>C	ENSP00000436430.2:p.Arg52Thr
ENST00000672314.2:c.532G>C	ENSP00000500828.2:p.Glu178Gln
ENST00000674679.2:c.*444G>C	ENSP00000501623.2:n.*444G>C
ENST00000710952.2:c.616G>C MANE Plus Clinical	ENSP00000518552.2:p.Glu206Gln
ENST00000672818.3:c.607G>C	ENSP00000500891.1:p.Glu203Gln
ENST00000450313.6:c.542G>C	ENSP00000408176.2:p.Arg181Thr
ENST00000456914.7:c.532G>C MANE Select	ENSP00000407590.2:p.Glu178Gln
ENST00000461495.6:c.*271G>C	ENSP00000437166.1:n.*271G>C
ENST00000671856.1:n.478G>C
ENST00000671898.1:c.1120G>C	ENSP00000499896.1:p.Glu374Gln
ENST00000672011.1:c.500G>C	ENSP00000500418.1:p.Arg167Thr
ENST00000672314.1:c.532G>C	ENSP00000500828.1:p.Glu178Gln
ENST00000672593.1:c.*420G>C	ENSP00000500455.1:n.*420G>C
ENST00000672764.1:c.491G>C	ENSP00000500886.1:p.Arg164Thr
ENST00000672818.2:c.607G>C	ENSP00000500891.1:p.Glu203Gln
ENST00000673134.1:c.*229G>C	ENSP00000500526.1:n.*229G>C
ENST00000674679.1:c.560G>C	ENSP00000501623.1:n.560G>C
ENST00000354383.10:c.535G>C	ENSP00000346354.6:p.Glu179Gln
ENST00000355498.6:c.532G>C	ENSP00000347685.2:p.Glu178Gln
ENST00000372098.7:c.607G>C	ENSP00000361170.3:p.Glu203Gln
ENST00000372104.5:c.532G>C	ENSP00000361176.1:p.Glu178Gln
ENST00000372110.7:c.577G>C	ENSP00000361182.3:p.Glu193Gln
ENST00000372115.7:c.574G>C	ENSP00000361187.3:p.Glu192Gln
ENST00000412971.5:c.148G>C	ENSP00000410263.1:p.Glu50Gln
ENST00000435155.1:c.565G>C	ENSP00000403655.1:p.Glu189Gln
ENST00000448481.5:c.565G>C	ENSP00000409718.1:p.Glu189Gln
ENST00000450313.5:c.616G>C	ENSP00000408176.1:p.Glu206Gln
ENST00000456914.6:c.532G>C	ENSP00000407590.2:p.Glu178Gln
ENST00000461495.5:c.*271G>C	ENSP00000437166.1:n.*271G>C
ENST00000462388.5:n.223G>C
ENST00000467940.5:c.*455G>C	ENSP00000436478.1:n.*455G>C
ENST00000470256.5:c.419G>C	ENSP00000434985.1:p.Arg140Thr
ENST00000475516.5:c.*345G>C	ENSP00000433843.1:n.*345G>C
ENST00000478796.5:n.519G>C
ENST00000479746.6:n.890G>C
ENST00000481571.5:c.*345G>C	ENSP00000436597.1:n.*345G>C
ENST00000483642.5:n.1047G>C
ENST00000488731.6:c.187+115G>C	ENSP00000432330.1:n.187+115G>C
ENST00000492494.5:n.929G>C
ENST00000525160.5:c.*183G>C	ENSP00000431568.1:n.*183G>C
ENST00000528013.6:c.574G>C	ENSP00000433130.2:p.Glu192Gln
ENST00000529984.5:c.187+115G>C	ENSP00000437093.1:n.187+115G>C
ENST00000531105.5:c.115+1743G>C	ENSP00000431292.1:n.115+1743G>C
ENST00000533178.5:c.161G>C	ENSP00000436430.1:p.Arg54Thr
NM_001048171.1:c.574G>C	NP_001041636.1:p.Glu192Gln
NM_001048172.1:c.535G>C	NP_001041637.1:p.Glu179Gln
NM_001048173.1:c.532G>C	NP_001041638.1:p.Glu178Gln
NM_001048174.1:c.532G>C	NP_001041639.1:p.Glu178Gln
NM_001128425.1:c.616G>C , LRG_220t1:c.616G>C	NP_001121897.1:p.Glu206Gln
NM_001293190.1:c.577G>C	NP_001280119.1:p.Glu193Gln
NM_001293191.1:c.565G>C	NP_001280120.1:p.Glu189Gln
NM_001293192.1:c.256G>C	NP_001280121.1:p.Glu86Gln
NM_001293195.1:c.532G>C	NP_001280124.1:p.Glu178Gln
NM_001293196.1:c.256G>C	NP_001280125.1:p.Glu86Gln
NM_012222.2:c.607G>C	NP_036354.1:p.Glu203Gln
XM_011541497.1:c.592G>C	XP_011539799.1:p.Glu198Gln
XM_011541498.1:c.574G>C	XP_011539800.1:p.Glu192Gln
XM_011541499.1:c.574G>C	XP_011539801.1:p.Glu192Gln
XM_011541500.1:c.574G>C	XP_011539802.1:p.Glu192Gln
XM_011541501.1:c.574G>C	XP_011539803.1:p.Glu192Gln
XM_011541502.1:c.574G>C	XP_011539804.1:p.Glu192Gln
XM_011541503.1:c.574G>C	XP_011539805.1:p.Glu192Gln
XM_011541504.1:c.565G>C	XP_011539806.1:p.Glu189Gln
XM_011541505.1:c.154G>C	XP_011539807.1:p.Glu52Gln
XM_011541506.1:c.154G>C	XP_011539808.1:p.Glu52Gln
XM_011541507.1:c.145G>C	XP_011539809.1:p.Glu49Gln
XM_011541508.1:c.160G>C	XP_011539810.1:p.Glu54Gln
XR_946658.1:n.663G>C
NM_001350650.1:c.187G>C	NP_001337579.1:p.Glu63Gln
NM_001350651.1:c.187G>C	NP_001337580.1:p.Glu63Gln
NR_146882.1:n.790G>C
NR_146883.1:n.604G>C
XM_011541497.3:c.592G>C	XP_011539799.1:p.Glu198Gln
XM_011541500.3:c.574G>C	XP_011539802.1:p.Glu192Gln
XM_011541501.2:c.574G>C	XP_011539803.1:p.Glu192Gln
XM_011541502.2:c.574G>C	XP_011539804.1:p.Glu192Gln
XM_011541503.2:c.574G>C	XP_011539805.1:p.Glu192Gln
XM_011541504.2:c.565G>C	XP_011539806.1:p.Glu189Gln
XM_011541505.2:c.154G>C	XP_011539807.1:p.Glu52Gln
XM_011541506.2:c.154G>C	XP_011539808.1:p.Glu52Gln
XM_017001331.1:c.574G>C	XP_016856820.1:p.Glu192Gln
XM_017001332.1:c.574G>C	XP_016856821.1:p.Glu192Gln
XM_017001333.1:c.574G>C	XP_016856822.1:p.Glu192Gln
XM_017001334.1:c.535G>C	XP_016856823.1:p.Glu179Gln
XM_017001335.1:c.256G>C	XP_016856824.1:p.Glu86Gln
XM_017001336.1:c.187G>C	XP_016856825.1:p.Glu63Gln
XM_017001337.1:c.187G>C	XP_016856826.1:p.Glu63Gln
XM_024447244.1:c.187G>C	XP_024303012.1:p.Glu63Gln
XM_024447245.1:c.187G>C	XP_024303013.1:p.Glu63Gln
XM_024447248.1:c.145G>C	XP_024303016.1:p.Glu49Gln
XM_024447249.1:c.16G>C	XP_024303017.1:p.Glu6Gln
XM_024447250.1:c.16G>C	XP_024303018.1:p.Glu6Gln
XM_024447251.1:c.16G>C	XP_024303019.1:p.Glu6Gln
XR_001737190.1:n.577G>C
XR_001737192.1:n.389G>C
XR_002956643.1:n.569G>C
XR_002956644.1:n.1104G>C
XR_946658.2:n.677G>C
NM_001048171.2:c.532G>C	NP_001041636.2:p.Glu178Gln
NM_001128425.2:c.616G>C MANE Plus Clinical	NP_001121897.1:p.Glu206Gln
NM_001048172.2:c.535G>C	NP_001041637.1:p.Glu179Gln
NM_001048173.2:c.532G>C	NP_001041638.1:p.Glu178Gln
NM_001048174.2:c.532G>C MANE Select	NP_001041639.1:p.Glu178Gln
NM_001293190.2:c.577G>C	NP_001280119.1:p.Glu193Gln
NM_001293191.2:c.565G>C	NP_001280120.1:p.Glu189Gln
NM_001293192.2:c.256G>C	NP_001280121.1:p.Glu86Gln
NM_001293195.2:c.532G>C	NP_001280124.1:p.Glu178Gln
NM_001293196.2:c.256G>C	NP_001280125.1:p.Glu86Gln
NM_001350650.2:c.187G>C	NP_001337579.1:p.Glu63Gln
NM_001350651.2:c.187G>C	NP_001337580.1:p.Glu63Gln
NM_012222.3:c.607G>C	NP_036354.1:p.Glu203Gln
NR_146882.2:n.760G>C
NR_146883.2:n.609G>C