Canonical Allele Identifier: CA375793251

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707481A>T (hg19) ; chr9:g.137813029A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813029A>T , CM000671.2:g.137813029A>T	GRCh38
NC_000009.11:g.140707481A>T , CM000671.1:g.140707481A>T	GRCh37
NC_000009.10:g.139827302A>T	NCBI36
NG_011776.1:g.199038A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2891A>T MANE Select	ENSP00000417980.1:p.Asp964Val
ENST00000636027.1:c.2777A>T	ENSP00000489961.1:p.Asp926Val
ENST00000637161.1:c.2798A>T	ENSP00000490328.1:p.Asp933Val
ENST00000637261.1:c.2931A>T	ENSP00000490815.1:n.2931A>T
ENST00000637891.1:c.785A>T	ENSP00000490907.1:p.Asp262Val
ENST00000460843.5:c.2891A>T	ENSP00000417980.1:p.Asp964Val
ENST00000462942.3:c.1748A>T	ENSP00000436107.1:p.Asp583Val
ENST00000486164.5:c.578A>T
ENST00000488242.2:n.417A>T
NM_024757.4:c.2891A>T	NP_079033.4:p.Asp964Val
XM_005266105.3:c.2882A>T	XP_005266162.1:p.Asp961Val
XM_005266110.1:c.2798A>T	XP_005266167.1:p.Asp933Val
XM_006717288.2:c.2873A>T	XP_006717351.1:p.Asp958Val
XM_011519021.1:c.2900A>T	XP_011517323.1:p.Asp967Val
XM_011519022.1:c.2897A>T	XP_011517324.1:p.Asp966Val
XM_011519023.1:c.2879A>T	XP_011517325.1:p.Asp960Val
XM_011519024.1:c.2822A>T	XP_011517326.1:p.Asp941Val
XM_011519025.1:c.2798A>T	XP_011517327.1:p.Asp933Val
XM_011519026.1:c.2756A>T	XP_011517328.1:p.Asp919Val
XM_011519029.1:c.1322A>T	XP_011517331.1:p.Asp441Val
XM_011519030.1:c.674A>T	XP_011517332.1:p.Asp225Val
XM_011519031.1:c.461A>T	XP_011517333.1:p.Asp154Val
XM_011519032.1:c.461A>T	XP_011517334.1:p.Asp154Val
XM_011519033.1:c.2735A>T	XP_011517335.1:p.Asp912Val
NM_001354263.1:c.2870A>T	NP_001341192.1:p.Asp957Val
XM_005266105.5:c.2882A>T	XP_005266162.1:p.Asp961Val
XM_011519021.3:c.2900A>T	XP_011517323.1:p.Asp967Val
XM_011519022.3:c.2897A>T	XP_011517324.1:p.Asp966Val
XM_011519023.3:c.2879A>T	XP_011517325.1:p.Asp960Val
XM_011519029.3:c.1322A>T	XP_011517331.1:p.Asp441Val
XM_011519030.3:c.674A>T	XP_011517332.1:p.Asp225Val
XM_017015134.1:c.2876A>T	XP_016870623.1:p.Asp959Val
XM_017015136.2:c.2792A>T	XP_016870625.1:p.Asp931Val
XM_017015137.1:c.2777A>T	XP_016870626.1:p.Asp926Val
XM_017015138.1:c.2777A>T	XP_016870627.1:p.Asp926Val
XM_024447674.1:c.2720A>T	XP_024303442.1:p.Asp907Val
XM_024447675.1:c.2654A>T	XP_024303443.1:p.Asp885Val
XM_024447676.1:c.2015A>T	XP_024303444.1:p.Asp672Val
XM_024447677.1:c.2015A>T	XP_024303445.1:p.Asp672Val
XM_024447680.1:c.2633A>T	XP_024303448.1:p.Asp878Val
NM_024757.5:c.2891A>T MANE Select	NP_079033.4:p.Asp964Val
NM_001354263.2:c.2870A>T	NP_001341192.1:p.Asp957Val