Canonical Allele Identifier: CA375793501

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707547G>A (hg19) ; chr9:g.137813095G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813095G>A , CM000671.2:g.137813095G>A	GRCh38
NC_000009.11:g.140707547G>A , CM000671.1:g.140707547G>A	GRCh37
NC_000009.10:g.139827368G>A	NCBI36
NG_011776.1:g.199104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2957G>A MANE Select	ENSP00000417980.1:p.Trp986Ter
ENST00000636027.1:c.2843G>A	ENSP00000489961.1:p.Trp948Ter
ENST00000637161.1:c.2864G>A	ENSP00000490328.1:p.Trp955Ter
ENST00000637261.1:c.2997G>A	ENSP00000490815.1:n.2997G>A
ENST00000637891.1:c.851G>A	ENSP00000490907.1:p.Trp284Ter
ENST00000460843.5:c.2957G>A	ENSP00000417980.1:p.Trp986Ter
ENST00000462942.3:c.1814G>A	ENSP00000436107.1:p.Trp605Ter
ENST00000486164.5:c.644G>A
ENST00000488242.2:n.483G>A
NM_024757.4:c.2957G>A	NP_079033.4:p.Trp986Ter
XM_005266105.3:c.2948G>A	XP_005266162.1:p.Trp983Ter
XM_005266110.1:c.2864G>A	XP_005266167.1:p.Trp955Ter
XM_006717288.2:c.2939G>A	XP_006717351.1:p.Trp980Ter
XM_011519021.1:c.2966G>A	XP_011517323.1:p.Trp989Ter
XM_011519022.1:c.2963G>A	XP_011517324.1:p.Trp988Ter
XM_011519023.1:c.2945G>A	XP_011517325.1:p.Trp982Ter
XM_011519024.1:c.2888G>A	XP_011517326.1:p.Trp963Ter
XM_011519025.1:c.2864G>A	XP_011517327.1:p.Trp955Ter
XM_011519026.1:c.2822G>A	XP_011517328.1:p.Trp941Ter
XM_011519029.1:c.1388G>A	XP_011517331.1:p.Trp463Ter
XM_011519030.1:c.740G>A	XP_011517332.1:p.Trp247Ter
XM_011519031.1:c.527G>A	XP_011517333.1:p.Trp176Ter
XM_011519032.1:c.527G>A	XP_011517334.1:p.Trp176Ter
XM_011519033.1:c.2801G>A	XP_011517335.1:p.Trp934Ter
NM_001354263.1:c.2936G>A	NP_001341192.1:p.Trp979Ter
XM_005266105.5:c.2948G>A	XP_005266162.1:p.Trp983Ter
XM_011519021.3:c.2966G>A	XP_011517323.1:p.Trp989Ter
XM_011519022.3:c.2963G>A	XP_011517324.1:p.Trp988Ter
XM_011519023.3:c.2945G>A	XP_011517325.1:p.Trp982Ter
XM_011519029.3:c.1388G>A	XP_011517331.1:p.Trp463Ter
XM_011519030.3:c.740G>A	XP_011517332.1:p.Trp247Ter
XM_017015134.1:c.2942G>A	XP_016870623.1:p.Trp981Ter
XM_017015136.2:c.2858G>A	XP_016870625.1:p.Trp953Ter
XM_017015137.1:c.2843G>A	XP_016870626.1:p.Trp948Ter
XM_017015138.1:c.2843G>A	XP_016870627.1:p.Trp948Ter
XM_024447674.1:c.2786G>A	XP_024303442.1:p.Trp929Ter
XM_024447675.1:c.2720G>A	XP_024303443.1:p.Trp907Ter
XM_024447676.1:c.2081G>A	XP_024303444.1:p.Trp694Ter
XM_024447677.1:c.2081G>A	XP_024303445.1:p.Trp694Ter
XM_024447680.1:c.2699G>A	XP_024303448.1:p.Trp900Ter
NM_024757.5:c.2957G>A MANE Select	NP_079033.4:p.Trp986Ter
NM_001354263.2:c.2936G>A	NP_001341192.1:p.Trp979Ter