Canonical Allele Identifier: CA375793711

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707609G>A (hg19) ; chr9:g.137813157G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813157G>A , CM000671.2:g.137813157G>A	GRCh38
NC_000009.11:g.140707609G>A , CM000671.1:g.140707609G>A	GRCh37
NC_000009.10:g.139827430G>A	NCBI36
NG_011776.1:g.199166G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3019G>A MANE Select	ENSP00000417980.1:p.Glu1007Lys
ENST00000636027.1:c.2905G>A	ENSP00000489961.1:p.Glu969Lys
ENST00000637161.1:c.2926G>A	ENSP00000490328.1:p.Glu976Lys
ENST00000637261.1:c.3059G>A	ENSP00000490815.1:n.3059G>A
ENST00000637891.1:c.913G>A	ENSP00000490907.1:p.Glu305Lys
ENST00000460843.5:c.3019G>A	ENSP00000417980.1:p.Glu1007Lys
ENST00000462942.3:c.1876G>A	ENSP00000436107.1:p.Glu626Lys
ENST00000486164.5:c.706G>A
ENST00000488242.2:n.545G>A
NM_024757.4:c.3019G>A	NP_079033.4:p.Glu1007Lys
XM_005266105.3:c.3010G>A	XP_005266162.1:p.Glu1004Lys
XM_005266110.1:c.2926G>A	XP_005266167.1:p.Glu976Lys
XM_006717288.2:c.3001G>A	XP_006717351.1:p.Glu1001Lys
XM_011519021.1:c.3028G>A	XP_011517323.1:p.Glu1010Lys
XM_011519022.1:c.3025G>A	XP_011517324.1:p.Glu1009Lys
XM_011519023.1:c.3007G>A	XP_011517325.1:p.Glu1003Lys
XM_011519024.1:c.2950G>A	XP_011517326.1:p.Glu984Lys
XM_011519025.1:c.2926G>A	XP_011517327.1:p.Glu976Lys
XM_011519026.1:c.2884G>A	XP_011517328.1:p.Glu962Lys
XM_011519029.1:c.1450G>A	XP_011517331.1:p.Glu484Lys
XM_011519030.1:c.802G>A	XP_011517332.1:p.Glu268Lys
XM_011519031.1:c.589G>A	XP_011517333.1:p.Glu197Lys
XM_011519032.1:c.589G>A	XP_011517334.1:p.Glu197Lys
XM_011519033.1:c.2863G>A	XP_011517335.1:p.Glu955Lys
NM_001354263.1:c.2998G>A	NP_001341192.1:p.Glu1000Lys
XM_005266105.5:c.3010G>A	XP_005266162.1:p.Glu1004Lys
XM_011519021.3:c.3028G>A	XP_011517323.1:p.Glu1010Lys
XM_011519022.3:c.3025G>A	XP_011517324.1:p.Glu1009Lys
XM_011519023.3:c.3007G>A	XP_011517325.1:p.Glu1003Lys
XM_011519029.3:c.1450G>A	XP_011517331.1:p.Glu484Lys
XM_011519030.3:c.802G>A	XP_011517332.1:p.Glu268Lys
XM_017015134.1:c.3004G>A	XP_016870623.1:p.Glu1002Lys
XM_017015136.2:c.2920G>A	XP_016870625.1:p.Glu974Lys
XM_017015137.1:c.2905G>A	XP_016870626.1:p.Glu969Lys
XM_017015138.1:c.2905G>A	XP_016870627.1:p.Glu969Lys
XM_024447674.1:c.2848G>A	XP_024303442.1:p.Glu950Lys
XM_024447675.1:c.2782G>A	XP_024303443.1:p.Glu928Lys
XM_024447676.1:c.2143G>A	XP_024303444.1:p.Glu715Lys
XM_024447677.1:c.2143G>A	XP_024303445.1:p.Glu715Lys
XM_024447680.1:c.2761G>A	XP_024303448.1:p.Glu921Lys
NM_024757.5:c.3019G>A MANE Select	NP_079033.4:p.Glu1007Lys
NM_001354263.2:c.2998G>A	NP_001341192.1:p.Glu1000Lys