Canonical Allele Identifier: CA417701994

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45795029A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45329357A>G , CM000663.2:g.45329357A>G	GRCh38
NC_000001.10:g.45795029A>G , CM000663.1:g.45795029A>G	GRCh37
NC_000001.9:g.45567616A>G	NCBI36
NG_008189.1:g.16114T>C , LRG_220:g.16114T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.1131T>C	ENSP00000410263.2:p.Phe377=
ENST00000435155.2:c.1548T>C	ENSP00000403655.2:p.Phe516=
ENST00000467459.6:c.*377T>C	ENSP00000435889.2:n.*377T>C
ENST00000483127.2:c.1533T>C	ENSP00000436469.2:p.Phe511=
ENST00000485271.6:c.*258T>C	ENSP00000431264.2:n.*258T>C
ENST00000529892.6:c.1368T>C	ENSP00000432528.2:p.Phe456=
ENST00000533178.6:c.*844T>C	ENSP00000436430.2:n.*844T>C
ENST00000672314.2:c.1515T>C	ENSP00000500828.2:p.Phe505=
ENST00000710952.2:c.1599T>C MANE Plus Clinical	ENSP00000518552.2:p.Phe533=
ENST00000672818.3:c.1590T>C	ENSP00000500891.1:p.Phe530=
ENST00000456914.7:c.1515T>C MANE Select	ENSP00000407590.2:p.Phe505=
ENST00000671898.1:c.*258T>C	ENSP00000499896.1:n.*258T>C
ENST00000672011.1:c.*844T>C	ENSP00000500418.1:n.*844T>C
ENST00000672818.2:c.1590T>C	ENSP00000500891.1:p.Phe530=
ENST00000354383.10:c.1518T>C	ENSP00000346354.6:p.Phe506=
ENST00000355498.6:c.1515T>C	ENSP00000347685.2:p.Phe505=
ENST00000372098.7:c.1590T>C	ENSP00000361170.3:p.Phe530=
ENST00000372104.5:c.1515T>C	ENSP00000361176.1:p.Phe505=
ENST00000372110.7:c.1560T>C	ENSP00000361182.3:p.Phe520=
ENST00000372115.7:c.1557T>C	ENSP00000361187.3:p.Phe519=
ENST00000448481.5:c.1548T>C	ENSP00000409718.1:p.Phe516=
ENST00000450313.5:c.1599T>C	ENSP00000408176.1:p.Phe533=
ENST00000456914.6:c.1515T>C	ENSP00000407590.2:p.Phe505=
ENST00000467459.5:c.932T>C	ENSP00000435889.1:n.932T>C
ENST00000475516.5:c.*1328T>C	ENSP00000433843.1:n.*1328T>C
ENST00000481571.5:c.*1328T>C	ENSP00000436597.1:n.*1328T>C
ENST00000482094.5:n.836T>C
ENST00000485271.5:c.392T>C
ENST00000488731.6:c.600T>C	ENSP00000432330.1:p.Phe200=
ENST00000528013.6:c.1557T>C	ENSP00000433130.2:p.Phe519=
ENST00000529892.5:c.590T>C
ENST00000529984.5:c.600T>C	ENSP00000437093.1:p.Phe200=
ENST00000531105.5:c.*7T>C	ENSP00000431292.1:n.*7T>C
ENST00000533178.5:c.1144T>C	ENSP00000436430.1:n.1144T>C
NM_001048171.1:c.1557T>C	NP_001041636.1:p.Phe519=
NM_001048172.1:c.1518T>C	NP_001041637.1:p.Phe506=
NM_001048173.1:c.1515T>C	NP_001041638.1:p.Phe505=
NM_001048174.1:c.1515T>C	NP_001041639.1:p.Phe505=
NM_001128425.1:c.1599T>C , LRG_220t1:c.1599T>C	NP_001121897.1:p.Phe533=
NM_001293190.1:c.1560T>C	NP_001280119.1:p.Phe520=
NM_001293191.1:c.1548T>C	NP_001280120.1:p.Phe516=
NM_001293192.1:c.1239T>C	NP_001280121.1:p.Phe413=
NM_001293195.1:c.1515T>C	NP_001280124.1:p.Phe505=
NM_001293196.1:c.1239T>C	NP_001280125.1:p.Phe413=
NM_012222.2:c.1590T>C	NP_036354.1:p.Phe530=
XM_011541497.1:c.1575T>C	XP_011539799.1:p.Phe525=
XM_011541498.1:c.1557T>C	XP_011539800.1:p.Phe519=
XM_011541499.1:c.1557T>C	XP_011539801.1:p.Phe519=
XM_011541500.1:c.1557T>C	XP_011539802.1:p.Phe519=
XM_011541501.1:c.1557T>C	XP_011539803.1:p.Phe519=
XM_011541502.1:c.1557T>C	XP_011539804.1:p.Phe519=
XM_011541503.1:c.1557T>C	XP_011539805.1:p.Phe519=
XM_011541504.1:c.1548T>C	XP_011539806.1:p.Phe516=
XM_011541505.1:c.1137T>C	XP_011539807.1:p.Phe379=
XM_011541506.1:c.1137T>C	XP_011539808.1:p.Phe379=
XM_011541507.1:c.1128T>C	XP_011539809.1:p.Phe376=
XM_011541508.1:c.1143T>C	XP_011539810.1:p.Phe381=
XR_946658.1:n.1826T>C
NM_001350650.1:c.1170T>C	NP_001337579.1:p.Phe390=
NM_001350651.1:c.1170T>C	NP_001337580.1:p.Phe390=
NR_146882.1:n.1953T>C
NR_146883.1:n.1767T>C
XM_011541497.3:c.1575T>C	XP_011539799.1:p.Phe525=
XM_011541500.3:c.1557T>C	XP_011539802.1:p.Phe519=
XM_011541501.2:c.1557T>C	XP_011539803.1:p.Phe519=
XM_011541502.2:c.1557T>C	XP_011539804.1:p.Phe519=
XM_011541503.2:c.1557T>C	XP_011539805.1:p.Phe519=
XM_011541504.2:c.1548T>C	XP_011539806.1:p.Phe516=
XM_011541505.2:c.1137T>C	XP_011539807.1:p.Phe379=
XM_011541506.2:c.1137T>C	XP_011539808.1:p.Phe379=
XM_017001331.1:c.1557T>C	XP_016856820.1:p.Phe519=
XM_017001332.1:c.1557T>C	XP_016856821.1:p.Phe519=
XM_017001333.1:c.1557T>C	XP_016856822.1:p.Phe519=
XM_017001334.1:c.1518T>C	XP_016856823.1:p.Phe506=
XM_017001335.1:c.1239T>C	XP_016856824.1:p.Phe413=
XM_017001336.1:c.1170T>C	XP_016856825.1:p.Phe390=
XM_017001337.1:c.1170T>C	XP_016856826.1:p.Phe390=
XM_024447244.1:c.1170T>C	XP_024303012.1:p.Phe390=
XM_024447245.1:c.1170T>C	XP_024303013.1:p.Phe390=
XM_024447248.1:c.1128T>C	XP_024303016.1:p.Phe376=
XM_024447249.1:c.999T>C	XP_024303017.1:p.Phe333=
XM_024447250.1:c.999T>C	XP_024303018.1:p.Phe333=
XM_024447251.1:c.999T>C	XP_024303019.1:p.Phe333=
XR_001737190.1:n.1740T>C
XR_001737192.1:n.1552T>C
XR_002956643.1:n.1732T>C
XR_002956644.1:n.2267T>C
XR_946658.2:n.1840T>C
NM_001048171.2:c.1515T>C	NP_001041636.2:p.Phe505=
NM_001128425.2:c.1599T>C MANE Plus Clinical	NP_001121897.1:p.Phe533=
NM_001048172.2:c.1518T>C	NP_001041637.1:p.Phe506=
NM_001048173.2:c.1515T>C	NP_001041638.1:p.Phe505=
NM_001048174.2:c.1515T>C MANE Select	NP_001041639.1:p.Phe505=
NM_001293190.2:c.1560T>C	NP_001280119.1:p.Phe520=
NM_001293191.2:c.1548T>C	NP_001280120.1:p.Phe516=
NM_001293192.2:c.1239T>C	NP_001280121.1:p.Phe413=
NM_001293195.2:c.1515T>C	NP_001280124.1:p.Phe505=
NM_001293196.2:c.1239T>C	NP_001280125.1:p.Phe413=
NM_001350650.2:c.1170T>C	NP_001337579.1:p.Phe390=
NM_001350651.2:c.1170T>C	NP_001337580.1:p.Phe390=
NM_012222.3:c.1590T>C	NP_036354.1:p.Phe530=
NR_146882.2:n.1923T>C
NR_146883.2:n.1772T>C