Canonical Allele Identifier: CA375793404

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707522T>G (hg19) ; chr9:g.137813070T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813070T>G , CM000671.2:g.137813070T>G	GRCh38
NC_000009.11:g.140707522T>G , CM000671.1:g.140707522T>G	GRCh37
NC_000009.10:g.139827343T>G	NCBI36
NG_011776.1:g.199079T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2932T>G MANE Select	ENSP00000417980.1:p.Cys978Gly
ENST00000636027.1:c.2818T>G	ENSP00000489961.1:p.Cys940Gly
ENST00000637161.1:c.2839T>G	ENSP00000490328.1:p.Cys947Gly
ENST00000637261.1:c.2972T>G	ENSP00000490815.1:n.2972T>G
ENST00000637891.1:c.826T>G	ENSP00000490907.1:p.Cys276Gly
ENST00000460843.5:c.2932T>G	ENSP00000417980.1:p.Cys978Gly
ENST00000462942.3:c.1789T>G	ENSP00000436107.1:p.Cys597Gly
ENST00000486164.5:c.619T>G
ENST00000488242.2:n.458T>G
NM_024757.4:c.2932T>G	NP_079033.4:p.Cys978Gly
XM_005266105.3:c.2923T>G	XP_005266162.1:p.Cys975Gly
XM_005266110.1:c.2839T>G	XP_005266167.1:p.Cys947Gly
XM_006717288.2:c.2914T>G	XP_006717351.1:p.Cys972Gly
XM_011519021.1:c.2941T>G	XP_011517323.1:p.Cys981Gly
XM_011519022.1:c.2938T>G	XP_011517324.1:p.Cys980Gly
XM_011519023.1:c.2920T>G	XP_011517325.1:p.Cys974Gly
XM_011519024.1:c.2863T>G	XP_011517326.1:p.Cys955Gly
XM_011519025.1:c.2839T>G	XP_011517327.1:p.Cys947Gly
XM_011519026.1:c.2797T>G	XP_011517328.1:p.Cys933Gly
XM_011519029.1:c.1363T>G	XP_011517331.1:p.Cys455Gly
XM_011519030.1:c.715T>G	XP_011517332.1:p.Cys239Gly
XM_011519031.1:c.502T>G	XP_011517333.1:p.Cys168Gly
XM_011519032.1:c.502T>G	XP_011517334.1:p.Cys168Gly
XM_011519033.1:c.2776T>G	XP_011517335.1:p.Cys926Gly
NM_001354263.1:c.2911T>G	NP_001341192.1:p.Cys971Gly
XM_005266105.5:c.2923T>G	XP_005266162.1:p.Cys975Gly
XM_011519021.3:c.2941T>G	XP_011517323.1:p.Cys981Gly
XM_011519022.3:c.2938T>G	XP_011517324.1:p.Cys980Gly
XM_011519023.3:c.2920T>G	XP_011517325.1:p.Cys974Gly
XM_011519029.3:c.1363T>G	XP_011517331.1:p.Cys455Gly
XM_011519030.3:c.715T>G	XP_011517332.1:p.Cys239Gly
XM_017015134.1:c.2917T>G	XP_016870623.1:p.Cys973Gly
XM_017015136.2:c.2833T>G	XP_016870625.1:p.Cys945Gly
XM_017015137.1:c.2818T>G	XP_016870626.1:p.Cys940Gly
XM_017015138.1:c.2818T>G	XP_016870627.1:p.Cys940Gly
XM_024447674.1:c.2761T>G	XP_024303442.1:p.Cys921Gly
XM_024447675.1:c.2695T>G	XP_024303443.1:p.Cys899Gly
XM_024447676.1:c.2056T>G	XP_024303444.1:p.Cys686Gly
XM_024447677.1:c.2056T>G	XP_024303445.1:p.Cys686Gly
XM_024447680.1:c.2674T>G	XP_024303448.1:p.Cys892Gly
NM_024757.5:c.2932T>G MANE Select	NP_079033.4:p.Cys978Gly
NM_001354263.2:c.2911T>G	NP_001341192.1:p.Cys971Gly