Canonical Allele Identifier: CA340133945

Gene: MUTYH

Linked Data

• gnomAD v4: 1-45331849-G-T
• MyVariant Identifiers: chr1:g.45797521G>T (hg19) ; chr1:g.45331849G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331849G>T , CM000663.2:g.45331849G>T	GRCh38
NC_000001.10:g.45797521G>T , CM000663.1:g.45797521G>T	GRCh37
NC_000001.9:g.45570108G>T	NCBI36
NG_008189.1:g.13622C>A , LRG_220:g.13622C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.530C>A	ENSP00000410263.2:p.Ala177Asp
ENST00000435155.2:c.947C>A	ENSP00000403655.2:p.Ala316Asp
ENST00000467459.6:c.937C>A	ENSP00000435889.2:p.Leu313Ile
ENST00000483127.2:c.932C>A	ENSP00000436469.2:p.Ala311Asp
ENST00000485271.6:c.914C>A	ENSP00000431264.2:p.Ala305Asp
ENST00000529892.6:c.955+174C>A	ENSP00000432528.2:n.955+174C>A
ENST00000533178.6:c.*243C>A	ENSP00000436430.2:n.*243C>A
ENST00000672314.2:c.914C>A	ENSP00000500828.2:p.Ala305Asp
ENST00000710952.2:c.998C>A MANE Plus Clinical	ENSP00000518552.2:p.Ala333Asp
ENST00000672818.3:c.989C>A	ENSP00000500891.1:p.Ala330Asp
ENST00000456914.7:c.914C>A MANE Select	ENSP00000407590.2:p.Ala305Asp
ENST00000671898.1:c.1502C>A	ENSP00000499896.1:p.Ala501Asp
ENST00000672011.1:c.*243C>A	ENSP00000500418.1:n.*243C>A
ENST00000672314.1:c.914C>A	ENSP00000500828.1:p.Ala305Asp
ENST00000672593.1:c.*1140C>A	ENSP00000500455.1:n.*1140C>A
ENST00000672764.1:c.*243C>A	ENSP00000500886.1:n.*243C>A
ENST00000672818.2:c.989C>A	ENSP00000500891.1:p.Ala330Asp
ENST00000673134.1:c.*611C>A	ENSP00000500526.1:n.*611C>A
ENST00000354383.10:c.917C>A	ENSP00000346354.6:p.Ala306Asp
ENST00000355498.6:c.914C>A	ENSP00000347685.2:p.Ala305Asp
ENST00000372098.7:c.989C>A	ENSP00000361170.3:p.Ala330Asp
ENST00000372104.5:c.914C>A	ENSP00000361176.1:p.Ala305Asp
ENST00000372110.7:c.959C>A	ENSP00000361182.3:p.Ala320Asp
ENST00000372115.7:c.956C>A	ENSP00000361187.3:p.Ala319Asp
ENST00000412971.5:c.530C>A	ENSP00000410263.1:p.Ala177Asp
ENST00000448481.5:c.947C>A	ENSP00000409718.1:p.Ala316Asp
ENST00000450313.5:c.998C>A	ENSP00000408176.1:p.Ala333Asp
ENST00000456914.6:c.914C>A	ENSP00000407590.2:p.Ala305Asp
ENST00000462388.5:n.778C>A
ENST00000466231.1:n.279C>A
ENST00000467459.5:c.331C>A	ENSP00000435889.1:p.Leu111Ile
ENST00000475516.5:c.*727C>A	ENSP00000433843.1:n.*727C>A
ENST00000481571.5:c.*727C>A	ENSP00000436597.1:n.*727C>A
ENST00000482094.5:n.235C>A
ENST00000488731.6:c.188-293C>A	ENSP00000432330.1:n.188-293C>A
ENST00000528013.6:c.956C>A	ENSP00000433130.2:p.Ala319Asp
ENST00000529892.5:c.177+174C>A
ENST00000529984.5:c.188-293C>A	ENSP00000437093.1:n.188-293C>A
ENST00000531105.5:c.116-2412C>A	ENSP00000431292.1:n.116-2412C>A
ENST00000533178.5:c.543C>A	ENSP00000436430.1:n.543C>A
NM_001048171.1:c.956C>A	NP_001041636.1:p.Ala319Asp
NM_001048172.1:c.917C>A	NP_001041637.1:p.Ala306Asp
NM_001048173.1:c.914C>A	NP_001041638.1:p.Ala305Asp
NM_001048174.1:c.914C>A	NP_001041639.1:p.Ala305Asp
NM_001128425.1:c.998C>A , LRG_220t1:c.998C>A	NP_001121897.1:p.Ala333Asp
NM_001293190.1:c.959C>A	NP_001280119.1:p.Ala320Asp
NM_001293191.1:c.947C>A	NP_001280120.1:p.Ala316Asp
NM_001293192.1:c.638C>A	NP_001280121.1:p.Ala213Asp
NM_001293195.1:c.914C>A	NP_001280124.1:p.Ala305Asp
NM_001293196.1:c.638C>A	NP_001280125.1:p.Ala213Asp
NM_012222.2:c.989C>A	NP_036354.1:p.Ala330Asp
XM_011541497.1:c.974C>A	XP_011539799.1:p.Ala325Asp
XM_011541498.1:c.956C>A	XP_011539800.1:p.Ala319Asp
XM_011541499.1:c.956C>A	XP_011539801.1:p.Ala319Asp
XM_011541500.1:c.956C>A	XP_011539802.1:p.Ala319Asp
XM_011541501.1:c.956C>A	XP_011539803.1:p.Ala319Asp
XM_011541502.1:c.956C>A	XP_011539804.1:p.Ala319Asp
XM_011541503.1:c.956C>A	XP_011539805.1:p.Ala319Asp
XM_011541504.1:c.947C>A	XP_011539806.1:p.Ala316Asp
XM_011541505.1:c.536C>A	XP_011539807.1:p.Ala179Asp
XM_011541506.1:c.536C>A	XP_011539808.1:p.Ala179Asp
XM_011541507.1:c.527C>A	XP_011539809.1:p.Ala176Asp
XM_011541508.1:c.542C>A	XP_011539810.1:p.Ala181Asp
XR_946658.1:n.1045C>A
NM_001350650.1:c.569C>A	NP_001337579.1:p.Ala190Asp
NM_001350651.1:c.569C>A	NP_001337580.1:p.Ala190Asp
NR_146882.1:n.1172C>A
NR_146883.1:n.986C>A
XM_011541497.3:c.974C>A	XP_011539799.1:p.Ala325Asp
XM_011541500.3:c.956C>A	XP_011539802.1:p.Ala319Asp
XM_011541501.2:c.956C>A	XP_011539803.1:p.Ala319Asp
XM_011541502.2:c.956C>A	XP_011539804.1:p.Ala319Asp
XM_011541503.2:c.956C>A	XP_011539805.1:p.Ala319Asp
XM_011541504.2:c.947C>A	XP_011539806.1:p.Ala316Asp
XM_011541505.2:c.536C>A	XP_011539807.1:p.Ala179Asp
XM_011541506.2:c.536C>A	XP_011539808.1:p.Ala179Asp
XM_017001331.1:c.956C>A	XP_016856820.1:p.Ala319Asp
XM_017001332.1:c.956C>A	XP_016856821.1:p.Ala319Asp
XM_017001333.1:c.956C>A	XP_016856822.1:p.Ala319Asp
XM_017001334.1:c.917C>A	XP_016856823.1:p.Ala306Asp
XM_017001335.1:c.638C>A	XP_016856824.1:p.Ala213Asp
XM_017001336.1:c.569C>A	XP_016856825.1:p.Ala190Asp
XM_017001337.1:c.569C>A	XP_016856826.1:p.Ala190Asp
XM_024447244.1:c.569C>A	XP_024303012.1:p.Ala190Asp
XM_024447245.1:c.569C>A	XP_024303013.1:p.Ala190Asp
XM_024447248.1:c.527C>A	XP_024303016.1:p.Ala176Asp
XM_024447249.1:c.398C>A	XP_024303017.1:p.Ala133Asp
XM_024447250.1:c.398C>A	XP_024303018.1:p.Ala133Asp
XM_024447251.1:c.398C>A	XP_024303019.1:p.Ala133Asp
XR_001737190.1:n.959C>A
XR_001737192.1:n.771C>A
XR_002956643.1:n.951C>A
XR_002956644.1:n.1486C>A
XR_946658.2:n.1059C>A
NM_001048171.2:c.914C>A	NP_001041636.2:p.Ala305Asp
NM_001128425.2:c.998C>A MANE Plus Clinical	NP_001121897.1:p.Ala333Asp
NM_001048172.2:c.917C>A	NP_001041637.1:p.Ala306Asp
NM_001048173.2:c.914C>A	NP_001041638.1:p.Ala305Asp
NM_001048174.2:c.914C>A MANE Select	NP_001041639.1:p.Ala305Asp
NM_001293190.2:c.959C>A	NP_001280119.1:p.Ala320Asp
NM_001293191.2:c.947C>A	NP_001280120.1:p.Ala316Asp
NM_001293192.2:c.638C>A	NP_001280121.1:p.Ala213Asp
NM_001293195.2:c.914C>A	NP_001280124.1:p.Ala305Asp
NM_001293196.2:c.638C>A	NP_001280125.1:p.Ala213Asp
NM_001350650.2:c.569C>A	NP_001337579.1:p.Ala190Asp
NM_001350651.2:c.569C>A	NP_001337580.1:p.Ala190Asp
NM_012222.3:c.989C>A	NP_036354.1:p.Ala330Asp
NR_146882.2:n.1142C>A
NR_146883.2:n.991C>A