Canonical Allele Identifier: CA375793661

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707583C>A (hg19) ; chr9:g.137813131C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813131C>A , CM000671.2:g.137813131C>A	GRCh38
NC_000009.11:g.140707583C>A , CM000671.1:g.140707583C>A	GRCh37
NC_000009.10:g.139827404C>A	NCBI36
NG_011776.1:g.199140C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2993C>A MANE Select	ENSP00000417980.1:p.Ser998Ter
ENST00000636027.1:c.2879C>A	ENSP00000489961.1:p.Ser960Ter
ENST00000637161.1:c.2900C>A	ENSP00000490328.1:p.Ser967Ter
ENST00000637261.1:c.3033C>A	ENSP00000490815.1:n.3033C>A
ENST00000637891.1:c.887C>A	ENSP00000490907.1:p.Ser296Ter
ENST00000460843.5:c.2993C>A	ENSP00000417980.1:p.Ser998Ter
ENST00000462942.3:c.1850C>A	ENSP00000436107.1:p.Ser617Ter
ENST00000486164.5:c.680C>A
ENST00000488242.2:n.519C>A
NM_024757.4:c.2993C>A	NP_079033.4:p.Ser998Ter
XM_005266105.3:c.2984C>A	XP_005266162.1:p.Ser995Ter
XM_005266110.1:c.2900C>A	XP_005266167.1:p.Ser967Ter
XM_006717288.2:c.2975C>A	XP_006717351.1:p.Ser992Ter
XM_011519021.1:c.3002C>A	XP_011517323.1:p.Ser1001Ter
XM_011519022.1:c.2999C>A	XP_011517324.1:p.Ser1000Ter
XM_011519023.1:c.2981C>A	XP_011517325.1:p.Ser994Ter
XM_011519024.1:c.2924C>A	XP_011517326.1:p.Ser975Ter
XM_011519025.1:c.2900C>A	XP_011517327.1:p.Ser967Ter
XM_011519026.1:c.2858C>A	XP_011517328.1:p.Ser953Ter
XM_011519029.1:c.1424C>A	XP_011517331.1:p.Ser475Ter
XM_011519030.1:c.776C>A	XP_011517332.1:p.Ser259Ter
XM_011519031.1:c.563C>A	XP_011517333.1:p.Ser188Ter
XM_011519032.1:c.563C>A	XP_011517334.1:p.Ser188Ter
XM_011519033.1:c.2837C>A	XP_011517335.1:p.Ser946Ter
NM_001354263.1:c.2972C>A	NP_001341192.1:p.Ser991Ter
XM_005266105.5:c.2984C>A	XP_005266162.1:p.Ser995Ter
XM_011519021.3:c.3002C>A	XP_011517323.1:p.Ser1001Ter
XM_011519022.3:c.2999C>A	XP_011517324.1:p.Ser1000Ter
XM_011519023.3:c.2981C>A	XP_011517325.1:p.Ser994Ter
XM_011519029.3:c.1424C>A	XP_011517331.1:p.Ser475Ter
XM_011519030.3:c.776C>A	XP_011517332.1:p.Ser259Ter
XM_017015134.1:c.2978C>A	XP_016870623.1:p.Ser993Ter
XM_017015136.2:c.2894C>A	XP_016870625.1:p.Ser965Ter
XM_017015137.1:c.2879C>A	XP_016870626.1:p.Ser960Ter
XM_017015138.1:c.2879C>A	XP_016870627.1:p.Ser960Ter
XM_024447674.1:c.2822C>A	XP_024303442.1:p.Ser941Ter
XM_024447675.1:c.2756C>A	XP_024303443.1:p.Ser919Ter
XM_024447676.1:c.2117C>A	XP_024303444.1:p.Ser706Ter
XM_024447677.1:c.2117C>A	XP_024303445.1:p.Ser706Ter
XM_024447680.1:c.2735C>A	XP_024303448.1:p.Ser912Ter
NM_024757.5:c.2993C>A MANE Select	NP_079033.4:p.Ser998Ter
NM_001354263.2:c.2972C>A	NP_001341192.1:p.Ser991Ter