Canonical Allele Identifier: CA375788833

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695369A>T (hg19) ; chr9:g.137800917A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800917A>T , CM000671.2:g.137800917A>T	GRCh38
NC_000009.11:g.140695369A>T , CM000671.1:g.140695369A>T	GRCh37
NC_000009.10:g.139815190A>T	NCBI36
NG_011776.1:g.186926A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2645A>T MANE Select	ENSP00000417980.1:p.Glu882Val
ENST00000636027.1:c.2531A>T	ENSP00000489961.1:p.Glu844Val
ENST00000637161.1:c.2552A>T	ENSP00000490328.1:p.Glu851Val
ENST00000637261.1:c.2685A>T	ENSP00000490815.1:n.2685A>T
ENST00000637891.1:c.539A>T	ENSP00000490907.1:p.Glu180Val
ENST00000637949.1:c.323A>T	ENSP00000489786.1:p.Glu108Val
ENST00000460843.5:c.2645A>T	ENSP00000417980.1:p.Glu882Val
ENST00000462942.3:c.1502A>T	ENSP00000436107.1:p.Glu501Val
ENST00000482340.5:c.215A>T	ENSP00000486748.1:p.Glu72Val
ENST00000486164.5:c.223A>T
ENST00000488242.2:n.171A>T
ENST00000493484.5:c.215A>T	ENSP00000486503.1:p.Glu72Val
NM_024757.4:c.2645A>T	NP_079033.4:p.Glu882Val
XM_005266105.3:c.2636A>T	XP_005266162.1:p.Glu879Val
XM_005266110.1:c.2552A>T	XP_005266167.1:p.Glu851Val
XM_006717288.2:c.2627A>T	XP_006717351.1:p.Glu876Val
XM_011519021.1:c.2654A>T	XP_011517323.1:p.Glu885Val
XM_011519022.1:c.2651A>T	XP_011517324.1:p.Glu884Val
XM_011519023.1:c.2633A>T	XP_011517325.1:p.Glu878Val
XM_011519024.1:c.2576A>T	XP_011517326.1:p.Glu859Val
XM_011519025.1:c.2552A>T	XP_011517327.1:p.Glu851Val
XM_011519026.1:c.2510A>T	XP_011517328.1:p.Glu837Val
XM_011519027.1:c.2654A>T	XP_011517329.1:p.Glu885Val
XM_011519029.1:c.1076A>T	XP_011517331.1:p.Glu359Val
XM_011519030.1:c.428A>T	XP_011517332.1:p.Glu143Val
XM_011519031.1:c.215A>T	XP_011517333.1:p.Glu72Val
XM_011519032.1:c.215A>T	XP_011517334.1:p.Glu72Val
XM_011519033.1:c.2489A>T	XP_011517335.1:p.Glu830Val
NM_001354263.1:c.2624A>T	NP_001341192.1:p.Glu875Val
XM_005266105.5:c.2636A>T	XP_005266162.1:p.Glu879Val
XM_011519021.3:c.2654A>T	XP_011517323.1:p.Glu885Val
XM_011519022.3:c.2651A>T	XP_011517324.1:p.Glu884Val
XM_011519023.3:c.2633A>T	XP_011517325.1:p.Glu878Val
XM_011519029.3:c.1076A>T	XP_011517331.1:p.Glu359Val
XM_011519030.3:c.428A>T	XP_011517332.1:p.Glu143Val
XM_017015134.1:c.2630A>T	XP_016870623.1:p.Glu877Val
XM_017015136.2:c.2546A>T	XP_016870625.1:p.Glu849Val
XM_017015137.1:c.2531A>T	XP_016870626.1:p.Glu844Val
XM_017015138.1:c.2531A>T	XP_016870627.1:p.Glu844Val
XM_024447674.1:c.2474A>T	XP_024303442.1:p.Glu825Val
XM_024447675.1:c.2408A>T	XP_024303443.1:p.Glu803Val
XM_024447676.1:c.1769A>T	XP_024303444.1:p.Glu590Val
XM_024447677.1:c.1769A>T	XP_024303445.1:p.Glu590Val
XM_024447678.1:c.2552A>T	XP_024303446.1:p.Glu851Val
XM_024447680.1:c.2387A>T	XP_024303448.1:p.Glu796Val
NM_024757.5:c.2645A>T MANE Select	NP_079033.4:p.Glu882Val
NM_001354263.2:c.2624A>T	NP_001341192.1:p.Glu875Val