Canonical Allele Identifier: CA375788922

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695390T>C (hg19) ; chr9:g.137800938T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800938T>C , CM000671.2:g.137800938T>C	GRCh38
NC_000009.11:g.140695390T>C , CM000671.1:g.140695390T>C	GRCh37
NC_000009.10:g.139815211T>C	NCBI36
NG_011776.1:g.186947T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2666T>C MANE Select	ENSP00000417980.1:p.Val889Ala
ENST00000636027.1:c.2552T>C	ENSP00000489961.1:p.Val851Ala
ENST00000637161.1:c.2573T>C	ENSP00000490328.1:p.Val858Ala
ENST00000637261.1:c.2706T>C	ENSP00000490815.1:n.2706T>C
ENST00000637891.1:c.560T>C	ENSP00000490907.1:p.Val187Ala
ENST00000637949.1:c.344T>C	ENSP00000489786.1:p.Val115Ala
ENST00000460843.5:c.2666T>C	ENSP00000417980.1:p.Val889Ala
ENST00000462942.3:c.1523T>C	ENSP00000436107.1:p.Val508Ala
ENST00000482340.5:c.236T>C	ENSP00000486748.1:p.Val79Ala
ENST00000486164.5:c.244T>C
ENST00000488242.2:n.192T>C
ENST00000493484.5:c.236T>C	ENSP00000486503.1:p.Val79Ala
NM_024757.4:c.2666T>C	NP_079033.4:p.Val889Ala
XM_005266105.3:c.2657T>C	XP_005266162.1:p.Val886Ala
XM_005266110.1:c.2573T>C	XP_005266167.1:p.Val858Ala
XM_006717288.2:c.2648T>C	XP_006717351.1:p.Val883Ala
XM_011519021.1:c.2675T>C	XP_011517323.1:p.Val892Ala
XM_011519022.1:c.2672T>C	XP_011517324.1:p.Val891Ala
XM_011519023.1:c.2654T>C	XP_011517325.1:p.Val885Ala
XM_011519024.1:c.2597T>C	XP_011517326.1:p.Val866Ala
XM_011519025.1:c.2573T>C	XP_011517327.1:p.Val858Ala
XM_011519026.1:c.2531T>C	XP_011517328.1:p.Val844Ala
XM_011519027.1:c.2675T>C	XP_011517329.1:p.Val892Ala
XM_011519029.1:c.1097T>C	XP_011517331.1:p.Val366Ala
XM_011519030.1:c.449T>C	XP_011517332.1:p.Val150Ala
XM_011519031.1:c.236T>C	XP_011517333.1:p.Val79Ala
XM_011519032.1:c.236T>C	XP_011517334.1:p.Val79Ala
XM_011519033.1:c.2510T>C	XP_011517335.1:p.Val837Ala
NM_001354263.1:c.2645T>C	NP_001341192.1:p.Val882Ala
XM_005266105.5:c.2657T>C	XP_005266162.1:p.Val886Ala
XM_011519021.3:c.2675T>C	XP_011517323.1:p.Val892Ala
XM_011519022.3:c.2672T>C	XP_011517324.1:p.Val891Ala
XM_011519023.3:c.2654T>C	XP_011517325.1:p.Val885Ala
XM_011519029.3:c.1097T>C	XP_011517331.1:p.Val366Ala
XM_011519030.3:c.449T>C	XP_011517332.1:p.Val150Ala
XM_017015134.1:c.2651T>C	XP_016870623.1:p.Val884Ala
XM_017015136.2:c.2567T>C	XP_016870625.1:p.Val856Ala
XM_017015137.1:c.2552T>C	XP_016870626.1:p.Val851Ala
XM_017015138.1:c.2552T>C	XP_016870627.1:p.Val851Ala
XM_024447674.1:c.2495T>C	XP_024303442.1:p.Val832Ala
XM_024447675.1:c.2429T>C	XP_024303443.1:p.Val810Ala
XM_024447676.1:c.1790T>C	XP_024303444.1:p.Val597Ala
XM_024447677.1:c.1790T>C	XP_024303445.1:p.Val597Ala
XM_024447678.1:c.2573T>C	XP_024303446.1:p.Val858Ala
XM_024447680.1:c.2408T>C	XP_024303448.1:p.Val803Ala
NM_024757.5:c.2666T>C MANE Select	NP_079033.4:p.Val889Ala
NM_001354263.2:c.2645T>C	NP_001341192.1:p.Val882Ala