Canonical Allele Identifier: CA375788856

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695374A>G (hg19) ; chr9:g.137800922A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800922A>G , CM000671.2:g.137800922A>G	GRCh38
NC_000009.11:g.140695374A>G , CM000671.1:g.140695374A>G	GRCh37
NC_000009.10:g.139815195A>G	NCBI36
NG_011776.1:g.186931A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2650A>G MANE Select	ENSP00000417980.1:p.Lys884Glu
ENST00000636027.1:c.2536A>G	ENSP00000489961.1:p.Lys846Glu
ENST00000637161.1:c.2557A>G	ENSP00000490328.1:p.Lys853Glu
ENST00000637261.1:c.2690A>G	ENSP00000490815.1:n.2690A>G
ENST00000637891.1:c.544A>G	ENSP00000490907.1:p.Lys182Glu
ENST00000637949.1:c.328A>G	ENSP00000489786.1:p.Lys110Glu
ENST00000460843.5:c.2650A>G	ENSP00000417980.1:p.Lys884Glu
ENST00000462942.3:c.1507A>G	ENSP00000436107.1:p.Lys503Glu
ENST00000482340.5:c.220A>G	ENSP00000486748.1:p.Lys74Glu
ENST00000486164.5:c.228A>G
ENST00000488242.2:n.176A>G
ENST00000493484.5:c.220A>G	ENSP00000486503.1:p.Lys74Glu
NM_024757.4:c.2650A>G	NP_079033.4:p.Lys884Glu
XM_005266105.3:c.2641A>G	XP_005266162.1:p.Lys881Glu
XM_005266110.1:c.2557A>G	XP_005266167.1:p.Lys853Glu
XM_006717288.2:c.2632A>G	XP_006717351.1:p.Lys878Glu
XM_011519021.1:c.2659A>G	XP_011517323.1:p.Lys887Glu
XM_011519022.1:c.2656A>G	XP_011517324.1:p.Lys886Glu
XM_011519023.1:c.2638A>G	XP_011517325.1:p.Lys880Glu
XM_011519024.1:c.2581A>G	XP_011517326.1:p.Lys861Glu
XM_011519025.1:c.2557A>G	XP_011517327.1:p.Lys853Glu
XM_011519026.1:c.2515A>G	XP_011517328.1:p.Lys839Glu
XM_011519027.1:c.2659A>G	XP_011517329.1:p.Lys887Glu
XM_011519029.1:c.1081A>G	XP_011517331.1:p.Lys361Glu
XM_011519030.1:c.433A>G	XP_011517332.1:p.Lys145Glu
XM_011519031.1:c.220A>G	XP_011517333.1:p.Lys74Glu
XM_011519032.1:c.220A>G	XP_011517334.1:p.Lys74Glu
XM_011519033.1:c.2494A>G	XP_011517335.1:p.Lys832Glu
NM_001354263.1:c.2629A>G	NP_001341192.1:p.Lys877Glu
XM_005266105.5:c.2641A>G	XP_005266162.1:p.Lys881Glu
XM_011519021.3:c.2659A>G	XP_011517323.1:p.Lys887Glu
XM_011519022.3:c.2656A>G	XP_011517324.1:p.Lys886Glu
XM_011519023.3:c.2638A>G	XP_011517325.1:p.Lys880Glu
XM_011519029.3:c.1081A>G	XP_011517331.1:p.Lys361Glu
XM_011519030.3:c.433A>G	XP_011517332.1:p.Lys145Glu
XM_017015134.1:c.2635A>G	XP_016870623.1:p.Lys879Glu
XM_017015136.2:c.2551A>G	XP_016870625.1:p.Lys851Glu
XM_017015137.1:c.2536A>G	XP_016870626.1:p.Lys846Glu
XM_017015138.1:c.2536A>G	XP_016870627.1:p.Lys846Glu
XM_024447674.1:c.2479A>G	XP_024303442.1:p.Lys827Glu
XM_024447675.1:c.2413A>G	XP_024303443.1:p.Lys805Glu
XM_024447676.1:c.1774A>G	XP_024303444.1:p.Lys592Glu
XM_024447677.1:c.1774A>G	XP_024303445.1:p.Lys592Glu
XM_024447678.1:c.2557A>G	XP_024303446.1:p.Lys853Glu
XM_024447680.1:c.2392A>G	XP_024303448.1:p.Lys798Glu
NM_024757.5:c.2650A>G MANE Select	NP_079033.4:p.Lys884Glu
NM_001354263.2:c.2629A>G	NP_001341192.1:p.Lys877Glu