Canonical Allele Identifier: CA375788733

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695344T>G (hg19) ; chr9:g.137800892T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800892T>G , CM000671.2:g.137800892T>G	GRCh38
NC_000009.11:g.140695344T>G , CM000671.1:g.140695344T>G	GRCh37
NC_000009.10:g.139815165T>G	NCBI36
NG_011776.1:g.186901T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2620T>G MANE Select	ENSP00000417980.1:p.Trp874Gly
ENST00000636027.1:c.2506T>G	ENSP00000489961.1:p.Trp836Gly
ENST00000637161.1:c.2527T>G	ENSP00000490328.1:p.Trp843Gly
ENST00000637261.1:c.2660T>G	ENSP00000490815.1:n.2660T>G
ENST00000637891.1:c.514T>G	ENSP00000490907.1:p.Trp172Gly
ENST00000637949.1:c.298T>G	ENSP00000489786.1:p.Trp100Gly
ENST00000460843.5:c.2620T>G	ENSP00000417980.1:p.Trp874Gly
ENST00000462942.3:c.1477T>G	ENSP00000436107.1:p.Trp493Gly
ENST00000482340.5:c.190T>G	ENSP00000486748.1:p.Trp64Gly
ENST00000486164.5:c.198T>G
ENST00000488242.2:n.146T>G
ENST00000493484.5:c.190T>G	ENSP00000486503.1:p.Trp64Gly
NM_024757.4:c.2620T>G	NP_079033.4:p.Trp874Gly
XM_005266105.3:c.2611T>G	XP_005266162.1:p.Trp871Gly
XM_005266110.1:c.2527T>G	XP_005266167.1:p.Trp843Gly
XM_006717288.2:c.2602T>G	XP_006717351.1:p.Trp868Gly
XM_011519021.1:c.2629T>G	XP_011517323.1:p.Trp877Gly
XM_011519022.1:c.2626T>G	XP_011517324.1:p.Trp876Gly
XM_011519023.1:c.2608T>G	XP_011517325.1:p.Trp870Gly
XM_011519024.1:c.2551T>G	XP_011517326.1:p.Trp851Gly
XM_011519025.1:c.2527T>G	XP_011517327.1:p.Trp843Gly
XM_011519026.1:c.2485T>G	XP_011517328.1:p.Trp829Gly
XM_011519027.1:c.2629T>G	XP_011517329.1:p.Trp877Gly
XM_011519029.1:c.1051T>G	XP_011517331.1:p.Trp351Gly
XM_011519030.1:c.403T>G	XP_011517332.1:p.Trp135Gly
XM_011519031.1:c.190T>G	XP_011517333.1:p.Trp64Gly
XM_011519032.1:c.190T>G	XP_011517334.1:p.Trp64Gly
XM_011519033.1:c.2464T>G	XP_011517335.1:p.Trp822Gly
NM_001354263.1:c.2599T>G	NP_001341192.1:p.Trp867Gly
XM_005266105.5:c.2611T>G	XP_005266162.1:p.Trp871Gly
XM_011519021.3:c.2629T>G	XP_011517323.1:p.Trp877Gly
XM_011519022.3:c.2626T>G	XP_011517324.1:p.Trp876Gly
XM_011519023.3:c.2608T>G	XP_011517325.1:p.Trp870Gly
XM_011519029.3:c.1051T>G	XP_011517331.1:p.Trp351Gly
XM_011519030.3:c.403T>G	XP_011517332.1:p.Trp135Gly
XM_017015134.1:c.2605T>G	XP_016870623.1:p.Trp869Gly
XM_017015136.2:c.2521T>G	XP_016870625.1:p.Trp841Gly
XM_017015137.1:c.2506T>G	XP_016870626.1:p.Trp836Gly
XM_017015138.1:c.2506T>G	XP_016870627.1:p.Trp836Gly
XM_024447674.1:c.2449T>G	XP_024303442.1:p.Trp817Gly
XM_024447675.1:c.2383T>G	XP_024303443.1:p.Trp795Gly
XM_024447676.1:c.1744T>G	XP_024303444.1:p.Trp582Gly
XM_024447677.1:c.1744T>G	XP_024303445.1:p.Trp582Gly
XM_024447678.1:c.2527T>G	XP_024303446.1:p.Trp843Gly
XM_024447680.1:c.2362T>G	XP_024303448.1:p.Trp788Gly
NM_024757.5:c.2620T>G MANE Select	NP_079033.4:p.Trp874Gly
NM_001354263.2:c.2599T>G	NP_001341192.1:p.Trp867Gly