Canonical Allele Identifier: CA375788710

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695337C>A (hg19) ; chr9:g.137800885C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800885C>A , CM000671.2:g.137800885C>A	GRCh38
NC_000009.11:g.140695337C>A , CM000671.1:g.140695337C>A	GRCh37
NC_000009.10:g.139815158C>A	NCBI36
NG_011776.1:g.186894C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2613C>A MANE Select	ENSP00000417980.1:p.Asp871Glu
ENST00000636027.1:c.2499C>A	ENSP00000489961.1:p.Asp833Glu
ENST00000637161.1:c.2520C>A	ENSP00000490328.1:p.Asp840Glu
ENST00000637261.1:c.2653C>A	ENSP00000490815.1:n.2653C>A
ENST00000637891.1:c.507C>A	ENSP00000490907.1:p.Asp169Glu
ENST00000637949.1:c.291C>A	ENSP00000489786.1:p.Asp97Glu
ENST00000460843.5:c.2613C>A	ENSP00000417980.1:p.Asp871Glu
ENST00000462942.3:c.1470C>A	ENSP00000436107.1:p.Asp490Glu
ENST00000482340.5:c.183C>A	ENSP00000486748.1:p.Asp61Glu
ENST00000486164.5:c.191C>A
ENST00000488242.2:n.139C>A
ENST00000493484.5:c.183C>A	ENSP00000486503.1:p.Asp61Glu
NM_024757.4:c.2613C>A	NP_079033.4:p.Asp871Glu
XM_005266105.3:c.2604C>A	XP_005266162.1:p.Asp868Glu
XM_005266110.1:c.2520C>A	XP_005266167.1:p.Asp840Glu
XM_006717288.2:c.2595C>A	XP_006717351.1:p.Asp865Glu
XM_011519021.1:c.2622C>A	XP_011517323.1:p.Asp874Glu
XM_011519022.1:c.2619C>A	XP_011517324.1:p.Asp873Glu
XM_011519023.1:c.2601C>A	XP_011517325.1:p.Asp867Glu
XM_011519024.1:c.2544C>A	XP_011517326.1:p.Asp848Glu
XM_011519025.1:c.2520C>A	XP_011517327.1:p.Asp840Glu
XM_011519026.1:c.2478C>A	XP_011517328.1:p.Asp826Glu
XM_011519027.1:c.2622C>A	XP_011517329.1:p.Asp874Glu
XM_011519029.1:c.1044C>A	XP_011517331.1:p.Asp348Glu
XM_011519030.1:c.396C>A	XP_011517332.1:p.Asp132Glu
XM_011519031.1:c.183C>A	XP_011517333.1:p.Asp61Glu
XM_011519032.1:c.183C>A	XP_011517334.1:p.Asp61Glu
XM_011519033.1:c.2457C>A	XP_011517335.1:p.Asp819Glu
NM_001354263.1:c.2592C>A	NP_001341192.1:p.Asp864Glu
XM_005266105.5:c.2604C>A	XP_005266162.1:p.Asp868Glu
XM_011519021.3:c.2622C>A	XP_011517323.1:p.Asp874Glu
XM_011519022.3:c.2619C>A	XP_011517324.1:p.Asp873Glu
XM_011519023.3:c.2601C>A	XP_011517325.1:p.Asp867Glu
XM_011519029.3:c.1044C>A	XP_011517331.1:p.Asp348Glu
XM_011519030.3:c.396C>A	XP_011517332.1:p.Asp132Glu
XM_017015134.1:c.2598C>A	XP_016870623.1:p.Asp866Glu
XM_017015136.2:c.2514C>A	XP_016870625.1:p.Asp838Glu
XM_017015137.1:c.2499C>A	XP_016870626.1:p.Asp833Glu
XM_017015138.1:c.2499C>A	XP_016870627.1:p.Asp833Glu
XM_024447674.1:c.2442C>A	XP_024303442.1:p.Asp814Glu
XM_024447675.1:c.2376C>A	XP_024303443.1:p.Asp792Glu
XM_024447676.1:c.1737C>A	XP_024303444.1:p.Asp579Glu
XM_024447677.1:c.1737C>A	XP_024303445.1:p.Asp579Glu
XM_024447678.1:c.2520C>A	XP_024303446.1:p.Asp840Glu
XM_024447680.1:c.2355C>A	XP_024303448.1:p.Asp785Glu
NM_024757.5:c.2613C>A MANE Select	NP_079033.4:p.Asp871Glu
NM_001354263.2:c.2592C>A	NP_001341192.1:p.Asp864Glu