Canonical Allele Identifier: CA1884685699

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813096G= , CM000671.2:g.137813096G=	GRCh38
NC_000009.11:g.140707548G= , CM000671.1:g.140707548G=	GRCh37
NC_000009.10:g.139827369G=	NCBI36
NG_011776.1:g.199105G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2958G= MANE Select	ENSP00000417980.1:p.Trp986=
ENST00000636027.1:c.2844G=	ENSP00000489961.1:p.Trp948=
ENST00000637161.1:c.2865G=	ENSP00000490328.1:p.Trp955=
ENST00000637261.1:c.2998G=	ENSP00000490815.1:n.2998G=
ENST00000637891.1:c.852G=	ENSP00000490907.1:p.Trp284=
ENST00000460843.5:c.2958G=	ENSP00000417980.1:p.Trp986=
ENST00000462942.3:c.1815G=	ENSP00000436107.1:p.Trp605=
ENST00000486164.5:c.645G=
ENST00000488242.2:n.484G=
NM_024757.4:c.2958G=	NP_079033.4:p.Trp986=
XM_005266105.3:c.2949G=	XP_005266162.1:p.Trp983=
XM_005266110.1:c.2865G=	XP_005266167.1:p.Trp955=
XM_006717288.2:c.2940G=	XP_006717351.1:p.Trp980=
XM_011519021.1:c.2967G=	XP_011517323.1:p.Trp989=
XM_011519022.1:c.2964G=	XP_011517324.1:p.Trp988=
XM_011519023.1:c.2946G=	XP_011517325.1:p.Trp982=
XM_011519024.1:c.2889G=	XP_011517326.1:p.Trp963=
XM_011519025.1:c.2865G=	XP_011517327.1:p.Trp955=
XM_011519026.1:c.2823G=	XP_011517328.1:p.Trp941=
XM_011519029.1:c.1389G=	XP_011517331.1:p.Trp463=
XM_011519030.1:c.741G=	XP_011517332.1:p.Trp247=
XM_011519031.1:c.528G=	XP_011517333.1:p.Trp176=
XM_011519032.1:c.528G=	XP_011517334.1:p.Trp176=
XM_011519033.1:c.2802G=	XP_011517335.1:p.Trp934=
NM_001354263.1:c.2937G=	NP_001341192.1:p.Trp979=
XM_005266105.5:c.2949G=	XP_005266162.1:p.Trp983=
XM_011519021.3:c.2967G=	XP_011517323.1:p.Trp989=
XM_011519022.3:c.2964G=	XP_011517324.1:p.Trp988=
XM_011519023.3:c.2946G=	XP_011517325.1:p.Trp982=
XM_011519029.3:c.1389G=	XP_011517331.1:p.Trp463=
XM_011519030.3:c.741G=	XP_011517332.1:p.Trp247=
XM_017015134.1:c.2943G=	XP_016870623.1:p.Trp981=
XM_017015136.2:c.2859G=	XP_016870625.1:p.Trp953=
XM_017015137.1:c.2844G=	XP_016870626.1:p.Trp948=
XM_017015138.1:c.2844G=	XP_016870627.1:p.Trp948=
XM_024447674.1:c.2787G=	XP_024303442.1:p.Trp929=
XM_024447675.1:c.2721G=	XP_024303443.1:p.Trp907=
XM_024447676.1:c.2082G=	XP_024303444.1:p.Trp694=
XM_024447677.1:c.2082G=	XP_024303445.1:p.Trp694=
XM_024447680.1:c.2700G=	XP_024303448.1:p.Trp900=
NM_024757.5:c.2958G= MANE Select	NP_079033.4:p.Trp986=
NM_001354263.2:c.2937G=	NP_001341192.1:p.Trp979=