Canonical Allele Identifier: CA375788889

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695381T>A (hg19) ; chr9:g.137800929T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800929T>A , CM000671.2:g.137800929T>A	GRCh38
NC_000009.11:g.140695381T>A , CM000671.1:g.140695381T>A	GRCh37
NC_000009.10:g.139815202T>A	NCBI36
NG_011776.1:g.186938T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2657T>A MANE Select	ENSP00000417980.1:p.Val886Glu
ENST00000636027.1:c.2543T>A	ENSP00000489961.1:p.Val848Glu
ENST00000637161.1:c.2564T>A	ENSP00000490328.1:p.Val855Glu
ENST00000637261.1:c.2697T>A	ENSP00000490815.1:n.2697T>A
ENST00000637891.1:c.551T>A	ENSP00000490907.1:p.Val184Glu
ENST00000637949.1:c.335T>A	ENSP00000489786.1:p.Val112Glu
ENST00000460843.5:c.2657T>A	ENSP00000417980.1:p.Val886Glu
ENST00000462942.3:c.1514T>A	ENSP00000436107.1:p.Val505Glu
ENST00000482340.5:c.227T>A	ENSP00000486748.1:p.Val76Glu
ENST00000486164.5:c.235T>A
ENST00000488242.2:n.183T>A
ENST00000493484.5:c.227T>A	ENSP00000486503.1:p.Val76Glu
NM_024757.4:c.2657T>A	NP_079033.4:p.Val886Glu
XM_005266105.3:c.2648T>A	XP_005266162.1:p.Val883Glu
XM_005266110.1:c.2564T>A	XP_005266167.1:p.Val855Glu
XM_006717288.2:c.2639T>A	XP_006717351.1:p.Val880Glu
XM_011519021.1:c.2666T>A	XP_011517323.1:p.Val889Glu
XM_011519022.1:c.2663T>A	XP_011517324.1:p.Val888Glu
XM_011519023.1:c.2645T>A	XP_011517325.1:p.Val882Glu
XM_011519024.1:c.2588T>A	XP_011517326.1:p.Val863Glu
XM_011519025.1:c.2564T>A	XP_011517327.1:p.Val855Glu
XM_011519026.1:c.2522T>A	XP_011517328.1:p.Val841Glu
XM_011519027.1:c.2666T>A	XP_011517329.1:p.Val889Glu
XM_011519029.1:c.1088T>A	XP_011517331.1:p.Val363Glu
XM_011519030.1:c.440T>A	XP_011517332.1:p.Val147Glu
XM_011519031.1:c.227T>A	XP_011517333.1:p.Val76Glu
XM_011519032.1:c.227T>A	XP_011517334.1:p.Val76Glu
XM_011519033.1:c.2501T>A	XP_011517335.1:p.Val834Glu
NM_001354263.1:c.2636T>A	NP_001341192.1:p.Val879Glu
XM_005266105.5:c.2648T>A	XP_005266162.1:p.Val883Glu
XM_011519021.3:c.2666T>A	XP_011517323.1:p.Val889Glu
XM_011519022.3:c.2663T>A	XP_011517324.1:p.Val888Glu
XM_011519023.3:c.2645T>A	XP_011517325.1:p.Val882Glu
XM_011519029.3:c.1088T>A	XP_011517331.1:p.Val363Glu
XM_011519030.3:c.440T>A	XP_011517332.1:p.Val147Glu
XM_017015134.1:c.2642T>A	XP_016870623.1:p.Val881Glu
XM_017015136.2:c.2558T>A	XP_016870625.1:p.Val853Glu
XM_017015137.1:c.2543T>A	XP_016870626.1:p.Val848Glu
XM_017015138.1:c.2543T>A	XP_016870627.1:p.Val848Glu
XM_024447674.1:c.2486T>A	XP_024303442.1:p.Val829Glu
XM_024447675.1:c.2420T>A	XP_024303443.1:p.Val807Glu
XM_024447676.1:c.1781T>A	XP_024303444.1:p.Val594Glu
XM_024447677.1:c.1781T>A	XP_024303445.1:p.Val594Glu
XM_024447678.1:c.2564T>A	XP_024303446.1:p.Val855Glu
XM_024447680.1:c.2399T>A	XP_024303448.1:p.Val800Glu
NM_024757.5:c.2657T>A MANE Select	NP_079033.4:p.Val886Glu
NM_001354263.2:c.2636T>A	NP_001341192.1:p.Val879Glu