Canonical Allele Identifier: CA1884679288

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800960C= , CM000671.2:g.137800960C=	GRCh38
NC_000009.11:g.140695412C= , CM000671.1:g.140695412C=	GRCh37
NC_000009.10:g.139815233C=	NCBI36
NG_011776.1:g.186969C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2688C= MANE Select	ENSP00000417980.1:p.Gly896=
ENST00000636027.1:c.2574C=	ENSP00000489961.1:p.Gly858=
ENST00000637161.1:c.2595C=	ENSP00000490328.1:p.Gly865=
ENST00000637261.1:c.2728C=	ENSP00000490815.1:n.2728C=
ENST00000637891.1:c.582C=	ENSP00000490907.1:p.Gly194=
ENST00000637949.1:c.366C=	ENSP00000489786.1:p.Gly122=
ENST00000460843.5:c.2688C=	ENSP00000417980.1:p.Gly896=
ENST00000462942.3:c.1545C=	ENSP00000436107.1:p.Gly515=
ENST00000482340.5:c.258C=	ENSP00000486748.1:p.Gly86=
ENST00000486164.5:c.266C=
ENST00000488242.2:n.214C=
ENST00000493484.5:c.258C=	ENSP00000486503.1:p.Gly86=
NM_024757.4:c.2688C=	NP_079033.4:p.Gly896=
XM_005266105.3:c.2679C=	XP_005266162.1:p.Gly893=
XM_005266110.1:c.2595C=	XP_005266167.1:p.Gly865=
XM_006717288.2:c.2670C=	XP_006717351.1:p.Gly890=
XM_011519021.1:c.2697C=	XP_011517323.1:p.Gly899=
XM_011519022.1:c.2694C=	XP_011517324.1:p.Gly898=
XM_011519023.1:c.2676C=	XP_011517325.1:p.Gly892=
XM_011519024.1:c.2619C=	XP_011517326.1:p.Gly873=
XM_011519025.1:c.2595C=	XP_011517327.1:p.Gly865=
XM_011519026.1:c.2553C=	XP_011517328.1:p.Gly851=
XM_011519027.1:c.2697C=	XP_011517329.1:p.Gly899=
XM_011519029.1:c.1119C=	XP_011517331.1:p.Gly373=
XM_011519030.1:c.471C=	XP_011517332.1:p.Gly157=
XM_011519031.1:c.258C=	XP_011517333.1:p.Gly86=
XM_011519032.1:c.258C=	XP_011517334.1:p.Gly86=
XM_011519033.1:c.2532C=	XP_011517335.1:p.Gly844=
NM_001354263.1:c.2667C=	NP_001341192.1:p.Gly889=
XM_005266105.5:c.2679C=	XP_005266162.1:p.Gly893=
XM_011519021.3:c.2697C=	XP_011517323.1:p.Gly899=
XM_011519022.3:c.2694C=	XP_011517324.1:p.Gly898=
XM_011519023.3:c.2676C=	XP_011517325.1:p.Gly892=
XM_011519029.3:c.1119C=	XP_011517331.1:p.Gly373=
XM_011519030.3:c.471C=	XP_011517332.1:p.Gly157=
XM_017015134.1:c.2673C=	XP_016870623.1:p.Gly891=
XM_017015136.2:c.2589C=	XP_016870625.1:p.Gly863=
XM_017015137.1:c.2574C=	XP_016870626.1:p.Gly858=
XM_017015138.1:c.2574C=	XP_016870627.1:p.Gly858=
XM_024447674.1:c.2517C=	XP_024303442.1:p.Gly839=
XM_024447675.1:c.2451C=	XP_024303443.1:p.Gly817=
XM_024447676.1:c.1812C=	XP_024303444.1:p.Gly604=
XM_024447677.1:c.1812C=	XP_024303445.1:p.Gly604=
XM_024447678.1:c.2595C=	XP_024303446.1:p.Gly865=
XM_024447680.1:c.2430C=	XP_024303448.1:p.Gly810=
NM_024757.5:c.2688C= MANE Select	NP_079033.4:p.Gly896=
NM_001354263.2:c.2667C=	NP_001341192.1:p.Gly889=