Canonical Allele Identifier: CA375788774

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695355G>T (hg19) ; chr9:g.137800903G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800903G>T , CM000671.2:g.137800903G>T	GRCh38
NC_000009.11:g.140695355G>T , CM000671.1:g.140695355G>T	GRCh37
NC_000009.10:g.139815176G>T	NCBI36
NG_011776.1:g.186912G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2631G>T MANE Select	ENSP00000417980.1:p.Met877Ile
ENST00000636027.1:c.2517G>T	ENSP00000489961.1:p.Met839Ile
ENST00000637161.1:c.2538G>T	ENSP00000490328.1:p.Met846Ile
ENST00000637261.1:c.2671G>T	ENSP00000490815.1:n.2671G>T
ENST00000637891.1:c.525G>T	ENSP00000490907.1:p.Met175Ile
ENST00000637949.1:c.309G>T	ENSP00000489786.1:p.Met103Ile
ENST00000460843.5:c.2631G>T	ENSP00000417980.1:p.Met877Ile
ENST00000462942.3:c.1488G>T	ENSP00000436107.1:p.Met496Ile
ENST00000482340.5:c.201G>T	ENSP00000486748.1:p.Met67Ile
ENST00000486164.5:c.209G>T
ENST00000488242.2:n.157G>T
ENST00000493484.5:c.201G>T	ENSP00000486503.1:p.Met67Ile
NM_024757.4:c.2631G>T	NP_079033.4:p.Met877Ile
XM_005266105.3:c.2622G>T	XP_005266162.1:p.Met874Ile
XM_005266110.1:c.2538G>T	XP_005266167.1:p.Met846Ile
XM_006717288.2:c.2613G>T	XP_006717351.1:p.Met871Ile
XM_011519021.1:c.2640G>T	XP_011517323.1:p.Met880Ile
XM_011519022.1:c.2637G>T	XP_011517324.1:p.Met879Ile
XM_011519023.1:c.2619G>T	XP_011517325.1:p.Met873Ile
XM_011519024.1:c.2562G>T	XP_011517326.1:p.Met854Ile
XM_011519025.1:c.2538G>T	XP_011517327.1:p.Met846Ile
XM_011519026.1:c.2496G>T	XP_011517328.1:p.Met832Ile
XM_011519027.1:c.2640G>T	XP_011517329.1:p.Met880Ile
XM_011519029.1:c.1062G>T	XP_011517331.1:p.Met354Ile
XM_011519030.1:c.414G>T	XP_011517332.1:p.Met138Ile
XM_011519031.1:c.201G>T	XP_011517333.1:p.Met67Ile
XM_011519032.1:c.201G>T	XP_011517334.1:p.Met67Ile
XM_011519033.1:c.2475G>T	XP_011517335.1:p.Met825Ile
NM_001354263.1:c.2610G>T	NP_001341192.1:p.Met870Ile
XM_005266105.5:c.2622G>T	XP_005266162.1:p.Met874Ile
XM_011519021.3:c.2640G>T	XP_011517323.1:p.Met880Ile
XM_011519022.3:c.2637G>T	XP_011517324.1:p.Met879Ile
XM_011519023.3:c.2619G>T	XP_011517325.1:p.Met873Ile
XM_011519029.3:c.1062G>T	XP_011517331.1:p.Met354Ile
XM_011519030.3:c.414G>T	XP_011517332.1:p.Met138Ile
XM_017015134.1:c.2616G>T	XP_016870623.1:p.Met872Ile
XM_017015136.2:c.2532G>T	XP_016870625.1:p.Met844Ile
XM_017015137.1:c.2517G>T	XP_016870626.1:p.Met839Ile
XM_017015138.1:c.2517G>T	XP_016870627.1:p.Met839Ile
XM_024447674.1:c.2460G>T	XP_024303442.1:p.Met820Ile
XM_024447675.1:c.2394G>T	XP_024303443.1:p.Met798Ile
XM_024447676.1:c.1755G>T	XP_024303444.1:p.Met585Ile
XM_024447677.1:c.1755G>T	XP_024303445.1:p.Met585Ile
XM_024447678.1:c.2538G>T	XP_024303446.1:p.Met846Ile
XM_024447680.1:c.2373G>T	XP_024303448.1:p.Met791Ile
NM_024757.5:c.2631G>T MANE Select	NP_079033.4:p.Met877Ile
NM_001354263.2:c.2610G>T	NP_001341192.1:p.Met870Ile