Canonical Allele Identifier: CA375793215

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707474G>A (hg19) ; chr9:g.137813022G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813022G>A , CM000671.2:g.137813022G>A	GRCh38
NC_000009.11:g.140707474G>A , CM000671.1:g.140707474G>A	GRCh37
NC_000009.10:g.139827295G>A	NCBI36
NG_011776.1:g.199031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2884G>A MANE Select	ENSP00000417980.1:p.Asp962Asn
ENST00000636027.1:c.2770G>A	ENSP00000489961.1:p.Asp924Asn
ENST00000637161.1:c.2791G>A	ENSP00000490328.1:p.Asp931Asn
ENST00000637261.1:c.2924G>A	ENSP00000490815.1:n.2924G>A
ENST00000637891.1:c.778G>A	ENSP00000490907.1:p.Asp260Asn
ENST00000460843.5:c.2884G>A	ENSP00000417980.1:p.Asp962Asn
ENST00000462942.3:c.1741G>A	ENSP00000436107.1:p.Asp581Asn
ENST00000486164.5:c.571G>A
ENST00000488242.2:n.410G>A
NM_024757.4:c.2884G>A	NP_079033.4:p.Asp962Asn
XM_005266105.3:c.2875G>A	XP_005266162.1:p.Asp959Asn
XM_005266110.1:c.2791G>A	XP_005266167.1:p.Asp931Asn
XM_006717288.2:c.2866G>A	XP_006717351.1:p.Asp956Asn
XM_011519021.1:c.2893G>A	XP_011517323.1:p.Asp965Asn
XM_011519022.1:c.2890G>A	XP_011517324.1:p.Asp964Asn
XM_011519023.1:c.2872G>A	XP_011517325.1:p.Asp958Asn
XM_011519024.1:c.2815G>A	XP_011517326.1:p.Asp939Asn
XM_011519025.1:c.2791G>A	XP_011517327.1:p.Asp931Asn
XM_011519026.1:c.2749G>A	XP_011517328.1:p.Asp917Asn
XM_011519029.1:c.1315G>A	XP_011517331.1:p.Asp439Asn
XM_011519030.1:c.667G>A	XP_011517332.1:p.Asp223Asn
XM_011519031.1:c.454G>A	XP_011517333.1:p.Asp152Asn
XM_011519032.1:c.454G>A	XP_011517334.1:p.Asp152Asn
XM_011519033.1:c.2728G>A	XP_011517335.1:p.Asp910Asn
NM_001354263.1:c.2863G>A	NP_001341192.1:p.Asp955Asn
XM_005266105.5:c.2875G>A	XP_005266162.1:p.Asp959Asn
XM_011519021.3:c.2893G>A	XP_011517323.1:p.Asp965Asn
XM_011519022.3:c.2890G>A	XP_011517324.1:p.Asp964Asn
XM_011519023.3:c.2872G>A	XP_011517325.1:p.Asp958Asn
XM_011519029.3:c.1315G>A	XP_011517331.1:p.Asp439Asn
XM_011519030.3:c.667G>A	XP_011517332.1:p.Asp223Asn
XM_017015134.1:c.2869G>A	XP_016870623.1:p.Asp957Asn
XM_017015136.2:c.2785G>A	XP_016870625.1:p.Asp929Asn
XM_017015137.1:c.2770G>A	XP_016870626.1:p.Asp924Asn
XM_017015138.1:c.2770G>A	XP_016870627.1:p.Asp924Asn
XM_024447674.1:c.2713G>A	XP_024303442.1:p.Asp905Asn
XM_024447675.1:c.2647G>A	XP_024303443.1:p.Asp883Asn
XM_024447676.1:c.2008G>A	XP_024303444.1:p.Asp670Asn
XM_024447677.1:c.2008G>A	XP_024303445.1:p.Asp670Asn
XM_024447680.1:c.2626G>A	XP_024303448.1:p.Asp876Asn
NM_024757.5:c.2884G>A MANE Select	NP_079033.4:p.Asp962Asn
NM_001354263.2:c.2863G>A	NP_001341192.1:p.Asp955Asn