Canonical Allele Identifier: CA375793256

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707482T>G (hg19) ; chr9:g.137813030T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813030T>G , CM000671.2:g.137813030T>G	GRCh38
NC_000009.11:g.140707482T>G , CM000671.1:g.140707482T>G	GRCh37
NC_000009.10:g.139827303T>G	NCBI36
NG_011776.1:g.199039T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2892T>G MANE Select	ENSP00000417980.1:p.Asp964Glu
ENST00000636027.1:c.2778T>G	ENSP00000489961.1:p.Asp926Glu
ENST00000637161.1:c.2799T>G	ENSP00000490328.1:p.Asp933Glu
ENST00000637261.1:c.2932T>G	ENSP00000490815.1:n.2932T>G
ENST00000637891.1:c.786T>G	ENSP00000490907.1:p.Asp262Glu
ENST00000460843.5:c.2892T>G	ENSP00000417980.1:p.Asp964Glu
ENST00000462942.3:c.1749T>G	ENSP00000436107.1:p.Asp583Glu
ENST00000486164.5:c.579T>G
ENST00000488242.2:n.418T>G
NM_024757.4:c.2892T>G	NP_079033.4:p.Asp964Glu
XM_005266105.3:c.2883T>G	XP_005266162.1:p.Asp961Glu
XM_005266110.1:c.2799T>G	XP_005266167.1:p.Asp933Glu
XM_006717288.2:c.2874T>G	XP_006717351.1:p.Asp958Glu
XM_011519021.1:c.2901T>G	XP_011517323.1:p.Asp967Glu
XM_011519022.1:c.2898T>G	XP_011517324.1:p.Asp966Glu
XM_011519023.1:c.2880T>G	XP_011517325.1:p.Asp960Glu
XM_011519024.1:c.2823T>G	XP_011517326.1:p.Asp941Glu
XM_011519025.1:c.2799T>G	XP_011517327.1:p.Asp933Glu
XM_011519026.1:c.2757T>G	XP_011517328.1:p.Asp919Glu
XM_011519029.1:c.1323T>G	XP_011517331.1:p.Asp441Glu
XM_011519030.1:c.675T>G	XP_011517332.1:p.Asp225Glu
XM_011519031.1:c.462T>G	XP_011517333.1:p.Asp154Glu
XM_011519032.1:c.462T>G	XP_011517334.1:p.Asp154Glu
XM_011519033.1:c.2736T>G	XP_011517335.1:p.Asp912Glu
NM_001354263.1:c.2871T>G	NP_001341192.1:p.Asp957Glu
XM_005266105.5:c.2883T>G	XP_005266162.1:p.Asp961Glu
XM_011519021.3:c.2901T>G	XP_011517323.1:p.Asp967Glu
XM_011519022.3:c.2898T>G	XP_011517324.1:p.Asp966Glu
XM_011519023.3:c.2880T>G	XP_011517325.1:p.Asp960Glu
XM_011519029.3:c.1323T>G	XP_011517331.1:p.Asp441Glu
XM_011519030.3:c.675T>G	XP_011517332.1:p.Asp225Glu
XM_017015134.1:c.2877T>G	XP_016870623.1:p.Asp959Glu
XM_017015136.2:c.2793T>G	XP_016870625.1:p.Asp931Glu
XM_017015137.1:c.2778T>G	XP_016870626.1:p.Asp926Glu
XM_017015138.1:c.2778T>G	XP_016870627.1:p.Asp926Glu
XM_024447674.1:c.2721T>G	XP_024303442.1:p.Asp907Glu
XM_024447675.1:c.2655T>G	XP_024303443.1:p.Asp885Glu
XM_024447676.1:c.2016T>G	XP_024303444.1:p.Asp672Glu
XM_024447677.1:c.2016T>G	XP_024303445.1:p.Asp672Glu
XM_024447680.1:c.2634T>G	XP_024303448.1:p.Asp878Glu
NM_024757.5:c.2892T>G MANE Select	NP_079033.4:p.Asp964Glu
NM_001354263.2:c.2871T>G	NP_001341192.1:p.Asp957Glu