Canonical Allele Identifier: CA1884686464

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137814479C= , CM000671.2:g.137814479C=	GRCh38
NC_000009.11:g.140708931C= , CM000671.1:g.140708931C=	GRCh37
NC_000009.10:g.139828752C=	NCBI36
NG_011776.1:g.200488C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3229C= MANE Select	ENSP00000417980.1:p.Gln1077=
ENST00000637161.1:c.3136C=	ENSP00000490328.1:p.Gln1046=
ENST00000637261.1:c.3269C=	ENSP00000490815.1:n.3269C=
ENST00000637407.1:n.20C=
ENST00000637891.1:c.1303C=	ENSP00000490907.1:n.1303C=
ENST00000460843.5:c.3229C=	ENSP00000417980.1:p.Gln1077=
ENST00000462942.3:c.2086C=	ENSP00000436107.1:p.Gln696=
ENST00000483653.1:n.89C=
ENST00000488242.2:n.755C=
NM_024757.4:c.3229C=	NP_079033.4:p.Gln1077=
XM_005266105.3:c.3220C=	XP_005266162.1:p.Gln1074=
XM_005266110.1:c.3136C=	XP_005266167.1:p.Gln1046=
XM_006717288.2:c.3211C=	XP_006717351.1:p.Gln1071=
XM_011519021.1:c.3238C=	XP_011517323.1:p.Gln1080=
XM_011519022.1:c.3235C=	XP_011517324.1:p.Gln1079=
XM_011519023.1:c.3217C=	XP_011517325.1:p.Gln1073=
XM_011519024.1:c.3160C=	XP_011517326.1:p.Gln1054=
XM_011519025.1:c.3136C=	XP_011517327.1:p.Gln1046=
XM_011519026.1:c.3094C=	XP_011517328.1:p.Gln1032=
XM_011519029.1:c.1660C=	XP_011517331.1:p.Gln554=
XM_011519030.1:c.1012C=	XP_011517332.1:p.Gln338=
XM_011519031.1:c.799C=	XP_011517333.1:p.Gln267=
XM_011519032.1:c.799C=	XP_011517334.1:p.Gln267=
XM_011519033.1:c.3073C=	XP_011517335.1:p.Gln1025=
NM_001354263.1:c.3208C=	NP_001341192.1:p.Gln1070=
XM_005266105.5:c.3220C=	XP_005266162.1:p.Gln1074=
XM_011519021.3:c.3238C=	XP_011517323.1:p.Gln1080=
XM_011519022.3:c.3235C=	XP_011517324.1:p.Gln1079=
XM_011519023.3:c.3217C=	XP_011517325.1:p.Gln1073=
XM_011519029.3:c.1660C=	XP_011517331.1:p.Gln554=
XM_011519030.3:c.1012C=	XP_011517332.1:p.Gln338=
XM_017015134.1:c.3214C=	XP_016870623.1:p.Gln1072=
XM_017015136.2:c.3130C=	XP_016870625.1:p.Gln1044=
XM_017015137.1:c.3115C=	XP_016870626.1:p.Gln1039=
XM_017015138.1:c.3115C=	XP_016870627.1:p.Gln1039=
XM_024447674.1:c.3058C=	XP_024303442.1:p.Gln1020=
XM_024447675.1:c.2992C=	XP_024303443.1:p.Gln998=
XM_024447676.1:c.2353C=	XP_024303444.1:p.Gln785=
XM_024447677.1:c.2353C=	XP_024303445.1:p.Gln785=
XM_024447680.1:c.2971C=	XP_024303448.1:p.Gln991=
NM_024757.5:c.3229C= MANE Select	NP_079033.4:p.Gln1077=
NM_001354263.2:c.3208C=	NP_001341192.1:p.Gln1070=