Canonical Allele Identifier: CA1884685684

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813060G= , CM000671.2:g.137813060G=	GRCh38
NC_000009.11:g.140707512G= , CM000671.1:g.140707512G=	GRCh37
NC_000009.10:g.139827333G=	NCBI36
NG_011776.1:g.199069G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2922G= MANE Select	ENSP00000417980.1:p.Thr974=
ENST00000636027.1:c.2808G=	ENSP00000489961.1:p.Thr936=
ENST00000637161.1:c.2829G=	ENSP00000490328.1:p.Thr943=
ENST00000637261.1:c.2962G=	ENSP00000490815.1:n.2962G=
ENST00000637891.1:c.816G=	ENSP00000490907.1:p.Thr272=
ENST00000460843.5:c.2922G=	ENSP00000417980.1:p.Thr974=
ENST00000462942.3:c.1779G=	ENSP00000436107.1:p.Thr593=
ENST00000486164.5:c.609G=
ENST00000488242.2:n.448G=
NM_024757.4:c.2922G=	NP_079033.4:p.Thr974=
XM_005266105.3:c.2913G=	XP_005266162.1:p.Thr971=
XM_005266110.1:c.2829G=	XP_005266167.1:p.Thr943=
XM_006717288.2:c.2904G=	XP_006717351.1:p.Thr968=
XM_011519021.1:c.2931G=	XP_011517323.1:p.Thr977=
XM_011519022.1:c.2928G=	XP_011517324.1:p.Thr976=
XM_011519023.1:c.2910G=	XP_011517325.1:p.Thr970=
XM_011519024.1:c.2853G=	XP_011517326.1:p.Thr951=
XM_011519025.1:c.2829G=	XP_011517327.1:p.Thr943=
XM_011519026.1:c.2787G=	XP_011517328.1:p.Thr929=
XM_011519029.1:c.1353G=	XP_011517331.1:p.Thr451=
XM_011519030.1:c.705G=	XP_011517332.1:p.Thr235=
XM_011519031.1:c.492G=	XP_011517333.1:p.Thr164=
XM_011519032.1:c.492G=	XP_011517334.1:p.Thr164=
XM_011519033.1:c.2766G=	XP_011517335.1:p.Thr922=
NM_001354263.1:c.2901G=	NP_001341192.1:p.Thr967=
XM_005266105.5:c.2913G=	XP_005266162.1:p.Thr971=
XM_011519021.3:c.2931G=	XP_011517323.1:p.Thr977=
XM_011519022.3:c.2928G=	XP_011517324.1:p.Thr976=
XM_011519023.3:c.2910G=	XP_011517325.1:p.Thr970=
XM_011519029.3:c.1353G=	XP_011517331.1:p.Thr451=
XM_011519030.3:c.705G=	XP_011517332.1:p.Thr235=
XM_017015134.1:c.2907G=	XP_016870623.1:p.Thr969=
XM_017015136.2:c.2823G=	XP_016870625.1:p.Thr941=
XM_017015137.1:c.2808G=	XP_016870626.1:p.Thr936=
XM_017015138.1:c.2808G=	XP_016870627.1:p.Thr936=
XM_024447674.1:c.2751G=	XP_024303442.1:p.Thr917=
XM_024447675.1:c.2685G=	XP_024303443.1:p.Thr895=
XM_024447676.1:c.2046G=	XP_024303444.1:p.Thr682=
XM_024447677.1:c.2046G=	XP_024303445.1:p.Thr682=
XM_024447680.1:c.2664G=	XP_024303448.1:p.Thr888=
NM_024757.5:c.2922G= MANE Select	NP_079033.4:p.Thr974=
NM_001354263.2:c.2901G=	NP_001341192.1:p.Thr967=