Canonical Allele Identifier: CA375788788

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695358C>G (hg19) ; chr9:g.137800906C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800906C>G , CM000671.2:g.137800906C>G	GRCh38
NC_000009.11:g.140695358C>G , CM000671.1:g.140695358C>G	GRCh37
NC_000009.10:g.139815179C>G	NCBI36
NG_011776.1:g.186915C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2634C>G MANE Select	ENSP00000417980.1:p.Ile878Met
ENST00000636027.1:c.2520C>G	ENSP00000489961.1:p.Ile840Met
ENST00000637161.1:c.2541C>G	ENSP00000490328.1:p.Ile847Met
ENST00000637261.1:c.2674C>G	ENSP00000490815.1:n.2674C>G
ENST00000637891.1:c.528C>G	ENSP00000490907.1:p.Ile176Met
ENST00000637949.1:c.312C>G	ENSP00000489786.1:p.Ile104Met
ENST00000460843.5:c.2634C>G	ENSP00000417980.1:p.Ile878Met
ENST00000462942.3:c.1491C>G	ENSP00000436107.1:p.Ile497Met
ENST00000482340.5:c.204C>G	ENSP00000486748.1:p.Ile68Met
ENST00000486164.5:c.212C>G
ENST00000488242.2:n.160C>G
ENST00000493484.5:c.204C>G	ENSP00000486503.1:p.Ile68Met
NM_024757.4:c.2634C>G	NP_079033.4:p.Ile878Met
XM_005266105.3:c.2625C>G	XP_005266162.1:p.Ile875Met
XM_005266110.1:c.2541C>G	XP_005266167.1:p.Ile847Met
XM_006717288.2:c.2616C>G	XP_006717351.1:p.Ile872Met
XM_011519021.1:c.2643C>G	XP_011517323.1:p.Ile881Met
XM_011519022.1:c.2640C>G	XP_011517324.1:p.Ile880Met
XM_011519023.1:c.2622C>G	XP_011517325.1:p.Ile874Met
XM_011519024.1:c.2565C>G	XP_011517326.1:p.Ile855Met
XM_011519025.1:c.2541C>G	XP_011517327.1:p.Ile847Met
XM_011519026.1:c.2499C>G	XP_011517328.1:p.Ile833Met
XM_011519027.1:c.2643C>G	XP_011517329.1:p.Ile881Met
XM_011519029.1:c.1065C>G	XP_011517331.1:p.Ile355Met
XM_011519030.1:c.417C>G	XP_011517332.1:p.Ile139Met
XM_011519031.1:c.204C>G	XP_011517333.1:p.Ile68Met
XM_011519032.1:c.204C>G	XP_011517334.1:p.Ile68Met
XM_011519033.1:c.2478C>G	XP_011517335.1:p.Ile826Met
NM_001354263.1:c.2613C>G	NP_001341192.1:p.Ile871Met
XM_005266105.5:c.2625C>G	XP_005266162.1:p.Ile875Met
XM_011519021.3:c.2643C>G	XP_011517323.1:p.Ile881Met
XM_011519022.3:c.2640C>G	XP_011517324.1:p.Ile880Met
XM_011519023.3:c.2622C>G	XP_011517325.1:p.Ile874Met
XM_011519029.3:c.1065C>G	XP_011517331.1:p.Ile355Met
XM_011519030.3:c.417C>G	XP_011517332.1:p.Ile139Met
XM_017015134.1:c.2619C>G	XP_016870623.1:p.Ile873Met
XM_017015136.2:c.2535C>G	XP_016870625.1:p.Ile845Met
XM_017015137.1:c.2520C>G	XP_016870626.1:p.Ile840Met
XM_017015138.1:c.2520C>G	XP_016870627.1:p.Ile840Met
XM_024447674.1:c.2463C>G	XP_024303442.1:p.Ile821Met
XM_024447675.1:c.2397C>G	XP_024303443.1:p.Ile799Met
XM_024447676.1:c.1758C>G	XP_024303444.1:p.Ile586Met
XM_024447677.1:c.1758C>G	XP_024303445.1:p.Ile586Met
XM_024447678.1:c.2541C>G	XP_024303446.1:p.Ile847Met
XM_024447680.1:c.2376C>G	XP_024303448.1:p.Ile792Met
NM_024757.5:c.2634C>G MANE Select	NP_079033.4:p.Ile878Met
NM_001354263.2:c.2613C>G	NP_001341192.1:p.Ile871Met