Canonical Allele Identifier: CA375793387

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707519C>G (hg19) ; chr9:g.137813067C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813067C>G , CM000671.2:g.137813067C>G	GRCh38
NC_000009.11:g.140707519C>G , CM000671.1:g.140707519C>G	GRCh37
NC_000009.10:g.139827340C>G	NCBI36
NG_011776.1:g.199076C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2929C>G MANE Select	ENSP00000417980.1:p.Gln977Glu
ENST00000636027.1:c.2815C>G	ENSP00000489961.1:p.Gln939Glu
ENST00000637161.1:c.2836C>G	ENSP00000490328.1:p.Gln946Glu
ENST00000637261.1:c.2969C>G	ENSP00000490815.1:n.2969C>G
ENST00000637891.1:c.823C>G	ENSP00000490907.1:p.Gln275Glu
ENST00000460843.5:c.2929C>G	ENSP00000417980.1:p.Gln977Glu
ENST00000462942.3:c.1786C>G	ENSP00000436107.1:p.Gln596Glu
ENST00000486164.5:c.616C>G
ENST00000488242.2:n.455C>G
NM_024757.4:c.2929C>G	NP_079033.4:p.Gln977Glu
XM_005266105.3:c.2920C>G	XP_005266162.1:p.Gln974Glu
XM_005266110.1:c.2836C>G	XP_005266167.1:p.Gln946Glu
XM_006717288.2:c.2911C>G	XP_006717351.1:p.Gln971Glu
XM_011519021.1:c.2938C>G	XP_011517323.1:p.Gln980Glu
XM_011519022.1:c.2935C>G	XP_011517324.1:p.Gln979Glu
XM_011519023.1:c.2917C>G	XP_011517325.1:p.Gln973Glu
XM_011519024.1:c.2860C>G	XP_011517326.1:p.Gln954Glu
XM_011519025.1:c.2836C>G	XP_011517327.1:p.Gln946Glu
XM_011519026.1:c.2794C>G	XP_011517328.1:p.Gln932Glu
XM_011519029.1:c.1360C>G	XP_011517331.1:p.Gln454Glu
XM_011519030.1:c.712C>G	XP_011517332.1:p.Gln238Glu
XM_011519031.1:c.499C>G	XP_011517333.1:p.Gln167Glu
XM_011519032.1:c.499C>G	XP_011517334.1:p.Gln167Glu
XM_011519033.1:c.2773C>G	XP_011517335.1:p.Gln925Glu
NM_001354263.1:c.2908C>G	NP_001341192.1:p.Gln970Glu
XM_005266105.5:c.2920C>G	XP_005266162.1:p.Gln974Glu
XM_011519021.3:c.2938C>G	XP_011517323.1:p.Gln980Glu
XM_011519022.3:c.2935C>G	XP_011517324.1:p.Gln979Glu
XM_011519023.3:c.2917C>G	XP_011517325.1:p.Gln973Glu
XM_011519029.3:c.1360C>G	XP_011517331.1:p.Gln454Glu
XM_011519030.3:c.712C>G	XP_011517332.1:p.Gln238Glu
XM_017015134.1:c.2914C>G	XP_016870623.1:p.Gln972Glu
XM_017015136.2:c.2830C>G	XP_016870625.1:p.Gln944Glu
XM_017015137.1:c.2815C>G	XP_016870626.1:p.Gln939Glu
XM_017015138.1:c.2815C>G	XP_016870627.1:p.Gln939Glu
XM_024447674.1:c.2758C>G	XP_024303442.1:p.Gln920Glu
XM_024447675.1:c.2692C>G	XP_024303443.1:p.Gln898Glu
XM_024447676.1:c.2053C>G	XP_024303444.1:p.Gln685Glu
XM_024447677.1:c.2053C>G	XP_024303445.1:p.Gln685Glu
XM_024447680.1:c.2671C>G	XP_024303448.1:p.Gln891Glu
NM_024757.5:c.2929C>G MANE Select	NP_079033.4:p.Gln977Glu
NM_001354263.2:c.2908C>G	NP_001341192.1:p.Gln970Glu