Canonical Allele Identifier: CA375793218

Gene: EHMT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2884G>T MANE Select	ENSP00000417980.1:p.Asp962Tyr
ENST00000636027.1:c.2770G>T	ENSP00000489961.1:p.Asp924Tyr
ENST00000637161.1:c.2791G>T	ENSP00000490328.1:p.Asp931Tyr
ENST00000637261.1:c.2924G>T	ENSP00000490815.1:n.2924G>T
ENST00000637891.1:c.778G>T	ENSP00000490907.1:p.Asp260Tyr
ENST00000460843.5:c.2884G>T	ENSP00000417980.1:p.Asp962Tyr
ENST00000462942.3:c.1741G>T	ENSP00000436107.1:p.Asp581Tyr
ENST00000486164.5:c.571G>T
ENST00000488242.2:n.410G>T
NM_024757.4:c.2884G>T	NP_079033.4:p.Asp962Tyr
XM_005266105.3:c.2875G>T	XP_005266162.1:p.Asp959Tyr
XM_005266110.1:c.2791G>T	XP_005266167.1:p.Asp931Tyr
XM_006717288.2:c.2866G>T	XP_006717351.1:p.Asp956Tyr
XM_011519021.1:c.2893G>T	XP_011517323.1:p.Asp965Tyr
XM_011519022.1:c.2890G>T	XP_011517324.1:p.Asp964Tyr
XM_011519023.1:c.2872G>T	XP_011517325.1:p.Asp958Tyr
XM_011519024.1:c.2815G>T	XP_011517326.1:p.Asp939Tyr
XM_011519025.1:c.2791G>T	XP_011517327.1:p.Asp931Tyr
XM_011519026.1:c.2749G>T	XP_011517328.1:p.Asp917Tyr
XM_011519029.1:c.1315G>T	XP_011517331.1:p.Asp439Tyr
XM_011519030.1:c.667G>T	XP_011517332.1:p.Asp223Tyr
XM_011519031.1:c.454G>T	XP_011517333.1:p.Asp152Tyr
XM_011519032.1:c.454G>T	XP_011517334.1:p.Asp152Tyr
XM_011519033.1:c.2728G>T	XP_011517335.1:p.Asp910Tyr
NM_001354263.1:c.2863G>T	NP_001341192.1:p.Asp955Tyr
XM_005266105.5:c.2875G>T	XP_005266162.1:p.Asp959Tyr
XM_011519021.3:c.2893G>T	XP_011517323.1:p.Asp965Tyr
XM_011519022.3:c.2890G>T	XP_011517324.1:p.Asp964Tyr
XM_011519023.3:c.2872G>T	XP_011517325.1:p.Asp958Tyr
XM_011519029.3:c.1315G>T	XP_011517331.1:p.Asp439Tyr
XM_011519030.3:c.667G>T	XP_011517332.1:p.Asp223Tyr
XM_017015134.1:c.2869G>T	XP_016870623.1:p.Asp957Tyr
XM_017015136.2:c.2785G>T	XP_016870625.1:p.Asp929Tyr
XM_017015137.1:c.2770G>T	XP_016870626.1:p.Asp924Tyr
XM_017015138.1:c.2770G>T	XP_016870627.1:p.Asp924Tyr
XM_024447674.1:c.2713G>T	XP_024303442.1:p.Asp905Tyr
XM_024447675.1:c.2647G>T	XP_024303443.1:p.Asp883Tyr
XM_024447676.1:c.2008G>T	XP_024303444.1:p.Asp670Tyr
XM_024447677.1:c.2008G>T	XP_024303445.1:p.Asp670Tyr
XM_024447680.1:c.2626G>T	XP_024303448.1:p.Asp876Tyr
NM_024757.5:c.2884G>T MANE Select	NP_079033.4:p.Asp962Tyr
NM_001354263.2:c.2863G>T	NP_001341192.1:p.Asp955Tyr