Canonical Allele Identifier: CA1884650224

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137743418C= , CM000671.2:g.137743418C=	GRCh38
NC_000009.11:g.140637870C= , CM000671.1:g.140637870C=	GRCh37
NC_000009.10:g.139757691C=	NCBI36
NG_011776.1:g.129427C=

Transcript Alleles

HGVS	Amino-acid Change
NM_024757.5:c.871C= MANE Select	NP_079033.4:p.Arg291=
ENST00000460843.6:c.871C= MANE Select	ENSP00000417980.1:p.Arg291=
NM_001145527.1:c.871C=	NP_001138999.1:p.Arg291=
NM_001145527.2:c.871C=	NP_001138999.1:p.Arg291=
NM_001354259.1:c.778C=	NP_001341188.1:p.Arg260=
NM_001354259.2:c.778C=	NP_001341188.1:p.Arg260=
NM_001354263.1:c.850C=	NP_001341192.1:p.Arg284=
NM_001354263.2:c.850C=	NP_001341192.1:p.Arg284=
NM_001354611.1:c.871C=	NP_001341540.1:p.Arg291=
NM_001354611.2:c.871C=	NP_001341540.1:p.Arg291=
NM_001354612.1:c.778C=	NP_001341541.1:p.Arg260=
NM_001354612.2:c.778C=	NP_001341541.1:p.Arg260=
NM_024757.4:c.871C=	NP_079033.4:p.Arg291=
ENST00000371394.6:c.*606C=	ENSP00000485945.1:n.*606C=
ENST00000460843.5:c.871C=	ENSP00000417980.1:p.Arg291=
ENST00000462484.5:c.871C=	ENSP00000417328.1:p.Arg291=
ENST00000478940.1:n.162C=
ENST00000495657.5:n.221C=
ENST00000626066.2:c.774C=
ENST00000629335.2:c.871C=	ENSP00000490056.1:p.Arg291=
ENST00000629808.2:c.42C=
ENST00000636027.1:c.757C=	ENSP00000489961.1:p.Arg253=
ENST00000637161.1:c.778C=	ENSP00000490328.1:p.Arg260=
ENST00000637261.1:c.911C=	ENSP00000490815.1:n.911C=
ENST00000637318.1:c.-6C=	ENSP00000490611.1:n.-6C=
ENST00000637977.1:c.816C=
ENST00000638071.1:c.576C=
ENST00000640639.1:c.40C=	ENSP00000491823.1:p.Arg14=
XM_005266105.3:c.862C=	XP_005266162.1:p.Arg288=
XM_005266105.5:c.862C=	XP_005266162.1:p.Arg288=
XM_005266110.1:c.778C=	XP_005266167.1:p.Arg260=
XM_006717288.2:c.853C=	XP_006717351.1:p.Arg285=
XM_011519021.1:c.880C=	XP_011517323.1:p.Arg294=
XM_011519021.3:c.880C=	XP_011517323.1:p.Arg294=
XM_011519022.1:c.877C=	XP_011517324.1:p.Arg293=
XM_011519022.3:c.877C=	XP_011517324.1:p.Arg293=
XM_011519023.1:c.859C=	XP_011517325.1:p.Arg287=
XM_011519023.3:c.859C=	XP_011517325.1:p.Arg287=
XM_011519024.1:c.880C=	XP_011517326.1:p.Arg294=
XM_011519025.1:c.778C=	XP_011517327.1:p.Arg260=
XM_011519026.1:c.880C=	XP_011517328.1:p.Arg294=
XM_011519027.1:c.880C=	XP_011517329.1:p.Arg294=
XM_011519028.1:c.880C=	XP_011517330.1:p.Arg294=
XM_011519033.1:c.859C=	XP_011517335.1:p.Arg287=
XM_017015134.1:c.856C=	XP_016870623.1:p.Arg286=
XM_017015136.2:c.850C=	XP_016870625.1:p.Arg284=
XM_017015137.1:c.757C=	XP_016870626.1:p.Arg253=
XM_017015138.1:c.757C=	XP_016870627.1:p.Arg253=
XM_024447674.1:c.778C=	XP_024303442.1:p.Arg260=
XM_024447675.1:c.778C=	XP_024303443.1:p.Arg260=
XM_024447676.1:c.-6C=	XP_024303444.1:n.-6C=
XM_024447677.1:c.-6C=	XP_024303445.1:n.-6C=
XM_024447678.1:c.778C=	XP_024303446.1:p.Arg260=
XM_024447679.1:c.778C=	XP_024303447.1:p.Arg260=
XM_024447680.1:c.757C=	XP_024303448.1:p.Arg253=