Canonical Allele Identifier: CA375793413

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707524T>A (hg19) ; chr9:g.137813072T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813072T>A , CM000671.2:g.137813072T>A	GRCh38
NC_000009.11:g.140707524T>A , CM000671.1:g.140707524T>A	GRCh37
NC_000009.10:g.139827345T>A	NCBI36
NG_011776.1:g.199081T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2934T>A MANE Select	ENSP00000417980.1:p.Cys978Ter
ENST00000636027.1:c.2820T>A	ENSP00000489961.1:p.Cys940Ter
ENST00000637161.1:c.2841T>A	ENSP00000490328.1:p.Cys947Ter
ENST00000637261.1:c.2974T>A	ENSP00000490815.1:n.2974T>A
ENST00000637891.1:c.828T>A	ENSP00000490907.1:p.Cys276Ter
ENST00000460843.5:c.2934T>A	ENSP00000417980.1:p.Cys978Ter
ENST00000462942.3:c.1791T>A	ENSP00000436107.1:p.Cys597Ter
ENST00000486164.5:c.621T>A
ENST00000488242.2:n.460T>A
NM_024757.4:c.2934T>A	NP_079033.4:p.Cys978Ter
XM_005266105.3:c.2925T>A	XP_005266162.1:p.Cys975Ter
XM_005266110.1:c.2841T>A	XP_005266167.1:p.Cys947Ter
XM_006717288.2:c.2916T>A	XP_006717351.1:p.Cys972Ter
XM_011519021.1:c.2943T>A	XP_011517323.1:p.Cys981Ter
XM_011519022.1:c.2940T>A	XP_011517324.1:p.Cys980Ter
XM_011519023.1:c.2922T>A	XP_011517325.1:p.Cys974Ter
XM_011519024.1:c.2865T>A	XP_011517326.1:p.Cys955Ter
XM_011519025.1:c.2841T>A	XP_011517327.1:p.Cys947Ter
XM_011519026.1:c.2799T>A	XP_011517328.1:p.Cys933Ter
XM_011519029.1:c.1365T>A	XP_011517331.1:p.Cys455Ter
XM_011519030.1:c.717T>A	XP_011517332.1:p.Cys239Ter
XM_011519031.1:c.504T>A	XP_011517333.1:p.Cys168Ter
XM_011519032.1:c.504T>A	XP_011517334.1:p.Cys168Ter
XM_011519033.1:c.2778T>A	XP_011517335.1:p.Cys926Ter
NM_001354263.1:c.2913T>A	NP_001341192.1:p.Cys971Ter
XM_005266105.5:c.2925T>A	XP_005266162.1:p.Cys975Ter
XM_011519021.3:c.2943T>A	XP_011517323.1:p.Cys981Ter
XM_011519022.3:c.2940T>A	XP_011517324.1:p.Cys980Ter
XM_011519023.3:c.2922T>A	XP_011517325.1:p.Cys974Ter
XM_011519029.3:c.1365T>A	XP_011517331.1:p.Cys455Ter
XM_011519030.3:c.717T>A	XP_011517332.1:p.Cys239Ter
XM_017015134.1:c.2919T>A	XP_016870623.1:p.Cys973Ter
XM_017015136.2:c.2835T>A	XP_016870625.1:p.Cys945Ter
XM_017015137.1:c.2820T>A	XP_016870626.1:p.Cys940Ter
XM_017015138.1:c.2820T>A	XP_016870627.1:p.Cys940Ter
XM_024447674.1:c.2763T>A	XP_024303442.1:p.Cys921Ter
XM_024447675.1:c.2697T>A	XP_024303443.1:p.Cys899Ter
XM_024447676.1:c.2058T>A	XP_024303444.1:p.Cys686Ter
XM_024447677.1:c.2058T>A	XP_024303445.1:p.Cys686Ter
XM_024447680.1:c.2676T>A	XP_024303448.1:p.Cys892Ter
NM_024757.5:c.2934T>A MANE Select	NP_079033.4:p.Cys978Ter
NM_001354263.2:c.2913T>A	NP_001341192.1:p.Cys971Ter