Canonical Allele Identifier: CA375789083

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695436C>G (hg19) ; chr9:g.137800984C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800984C>G , CM000671.2:g.137800984C>G	GRCh38
NC_000009.11:g.140695436C>G , CM000671.1:g.140695436C>G	GRCh37
NC_000009.10:g.139815257C>G	NCBI36
NG_011776.1:g.186993C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2712C>G MANE Select	ENSP00000417980.1:p.Asn904Lys
ENST00000636027.1:c.2598C>G	ENSP00000489961.1:p.Asn866Lys
ENST00000637161.1:c.2619C>G	ENSP00000490328.1:p.Asn873Lys
ENST00000637261.1:c.2752C>G	ENSP00000490815.1:n.2752C>G
ENST00000637891.1:c.606C>G	ENSP00000490907.1:p.Asn202Lys
ENST00000637949.1:c.390C>G	ENSP00000489786.1:p.Asn130Lys
ENST00000460843.5:c.2712C>G	ENSP00000417980.1:p.Asn904Lys
ENST00000462942.3:c.1569C>G	ENSP00000436107.1:p.Asn523Lys
ENST00000482340.5:c.282C>G	ENSP00000486748.1:p.Asn94Lys
ENST00000486164.5:c.290C>G
ENST00000488242.2:n.238C>G
ENST00000493484.5:c.282C>G	ENSP00000486503.1:p.Asn94Lys
NM_024757.4:c.2712C>G	NP_079033.4:p.Asn904Lys
XM_005266105.3:c.2703C>G	XP_005266162.1:p.Asn901Lys
XM_005266110.1:c.2619C>G	XP_005266167.1:p.Asn873Lys
XM_006717288.2:c.2694C>G	XP_006717351.1:p.Asn898Lys
XM_011519021.1:c.2721C>G	XP_011517323.1:p.Asn907Lys
XM_011519022.1:c.2718C>G	XP_011517324.1:p.Asn906Lys
XM_011519023.1:c.2700C>G	XP_011517325.1:p.Asn900Lys
XM_011519024.1:c.2643C>G	XP_011517326.1:p.Asn881Lys
XM_011519025.1:c.2619C>G	XP_011517327.1:p.Asn873Lys
XM_011519026.1:c.2577C>G	XP_011517328.1:p.Asn859Lys
XM_011519027.1:c.2721C>G	XP_011517329.1:p.Asn907Lys
XM_011519029.1:c.1143C>G	XP_011517331.1:p.Asn381Lys
XM_011519030.1:c.495C>G	XP_011517332.1:p.Asn165Lys
XM_011519031.1:c.282C>G	XP_011517333.1:p.Asn94Lys
XM_011519032.1:c.282C>G	XP_011517334.1:p.Asn94Lys
XM_011519033.1:c.2556C>G	XP_011517335.1:p.Asn852Lys
NM_001354263.1:c.2691C>G	NP_001341192.1:p.Asn897Lys
XM_005266105.5:c.2703C>G	XP_005266162.1:p.Asn901Lys
XM_011519021.3:c.2721C>G	XP_011517323.1:p.Asn907Lys
XM_011519022.3:c.2718C>G	XP_011517324.1:p.Asn906Lys
XM_011519023.3:c.2700C>G	XP_011517325.1:p.Asn900Lys
XM_011519029.3:c.1143C>G	XP_011517331.1:p.Asn381Lys
XM_011519030.3:c.495C>G	XP_011517332.1:p.Asn165Lys
XM_017015134.1:c.2697C>G	XP_016870623.1:p.Asn899Lys
XM_017015136.2:c.2613C>G	XP_016870625.1:p.Asn871Lys
XM_017015137.1:c.2598C>G	XP_016870626.1:p.Asn866Lys
XM_017015138.1:c.2598C>G	XP_016870627.1:p.Asn866Lys
XM_024447674.1:c.2541C>G	XP_024303442.1:p.Asn847Lys
XM_024447675.1:c.2475C>G	XP_024303443.1:p.Asn825Lys
XM_024447676.1:c.1836C>G	XP_024303444.1:p.Asn612Lys
XM_024447677.1:c.1836C>G	XP_024303445.1:p.Asn612Lys
XM_024447678.1:c.2619C>G	XP_024303446.1:p.Asn873Lys
XM_024447680.1:c.2454C>G	XP_024303448.1:p.Asn818Lys
NM_024757.5:c.2712C>G MANE Select	NP_079033.4:p.Asn904Lys
NM_001354263.2:c.2691C>G	NP_001341192.1:p.Asn897Lys