Canonical Allele Identifier: CA467878104

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140705966C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137811514C>G , CM000671.2:g.137811514C>G	GRCh38
NC_000009.11:g.140705966C>G , CM000671.1:g.140705966C>G	GRCh37
NC_000009.10:g.139825787C>G	NCBI36
NG_011776.1:g.197523C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.2766C>G MANE Select	ENSP00000417980.1:p.Ala922=
ENST00000636027.1:c.2652C>G	ENSP00000489961.1:p.Ala884=
ENST00000637161.1:c.2673C>G	ENSP00000490328.1:p.Ala891=
ENST00000637261.1:c.2806C>G	ENSP00000490815.1:n.2806C>G
ENST00000637891.1:c.660C>G	ENSP00000490907.1:p.Ala220=
ENST00000460843.5:c.2766C>G	ENSP00000417980.1:p.Ala922=
ENST00000462942.3:c.1623C>G	ENSP00000436107.1:p.Ala541=
ENST00000486164.5:c.453C>G
ENST00000488242.2:n.292C>G
NM_024757.4:c.2766C>G	NP_079033.4:p.Ala922=
XM_005266105.3:c.2757C>G	XP_005266162.1:p.Ala919=
XM_005266110.1:c.2673C>G	XP_005266167.1:p.Ala891=
XM_006717288.2:c.2748C>G	XP_006717351.1:p.Ala916=
XM_011519021.1:c.2775C>G	XP_011517323.1:p.Ala925=
XM_011519022.1:c.2772C>G	XP_011517324.1:p.Ala924=
XM_011519023.1:c.2754C>G	XP_011517325.1:p.Ala918=
XM_011519024.1:c.2697C>G	XP_011517326.1:p.Ala899=
XM_011519025.1:c.2673C>G	XP_011517327.1:p.Ala891=
XM_011519026.1:c.2631C>G	XP_011517328.1:p.Ala877=
XM_011519029.1:c.1197C>G	XP_011517331.1:p.Ala399=
XM_011519030.1:c.549C>G	XP_011517332.1:p.Ala183=
XM_011519031.1:c.336C>G	XP_011517333.1:p.Ala112=
XM_011519032.1:c.336C>G	XP_011517334.1:p.Ala112=
XM_011519033.1:c.2610C>G	XP_011517335.1:p.Ala870=
NM_001354263.1:c.2745C>G	NP_001341192.1:p.Ala915=
XM_005266105.5:c.2757C>G	XP_005266162.1:p.Ala919=
XM_011519021.3:c.2775C>G	XP_011517323.1:p.Ala925=
XM_011519022.3:c.2772C>G	XP_011517324.1:p.Ala924=
XM_011519023.3:c.2754C>G	XP_011517325.1:p.Ala918=
XM_011519029.3:c.1197C>G	XP_011517331.1:p.Ala399=
XM_011519030.3:c.549C>G	XP_011517332.1:p.Ala183=
XM_017015134.1:c.2751C>G	XP_016870623.1:p.Ala917=
XM_017015136.2:c.2667C>G	XP_016870625.1:p.Ala889=
XM_017015137.1:c.2652C>G	XP_016870626.1:p.Ala884=
XM_017015138.1:c.2652C>G	XP_016870627.1:p.Ala884=
XM_024447674.1:c.2595C>G	XP_024303442.1:p.Ala865=
XM_024447675.1:c.2529C>G	XP_024303443.1:p.Ala843=
XM_024447676.1:c.1890C>G	XP_024303444.1:p.Ala630=
XM_024447677.1:c.1890C>G	XP_024303445.1:p.Ala630=
XM_024447680.1:c.2508C>G	XP_024303448.1:p.Ala836=
NM_024757.5:c.2766C>G MANE Select	NP_079033.4:p.Ala922=
NM_001354263.2:c.2745C>G	NP_001341192.1:p.Ala915=