Canonical Allele Identifier: CA375794537

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707960A>G (hg19) ; chr9:g.137813508A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813508A>G , CM000671.2:g.137813508A>G	GRCh38
NC_000009.11:g.140707960A>G , CM000671.1:g.140707960A>G	GRCh37
NC_000009.10:g.139827781A>G	NCBI36
NG_011776.1:g.199517A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3158A>G MANE Select	ENSP00000417980.1:p.Asp1053Gly
ENST00000637161.1:c.3065A>G	ENSP00000490328.1:p.Asp1022Gly
ENST00000637261.1:c.3198A>G	ENSP00000490815.1:n.3198A>G
ENST00000637891.1:c.1052A>G	ENSP00000490907.1:p.Asp351Gly
ENST00000460843.5:c.3158A>G	ENSP00000417980.1:p.Asp1053Gly
ENST00000462942.3:c.2015A>G	ENSP00000436107.1:p.Asp672Gly
ENST00000483653.1:n.18A>G
ENST00000488242.2:n.684A>G
NM_024757.4:c.3158A>G	NP_079033.4:p.Asp1053Gly
XM_005266105.3:c.3149A>G	XP_005266162.1:p.Asp1050Gly
XM_005266110.1:c.3065A>G	XP_005266167.1:p.Asp1022Gly
XM_006717288.2:c.3140A>G	XP_006717351.1:p.Asp1047Gly
XM_011519021.1:c.3167A>G	XP_011517323.1:p.Asp1056Gly
XM_011519022.1:c.3164A>G	XP_011517324.1:p.Asp1055Gly
XM_011519023.1:c.3146A>G	XP_011517325.1:p.Asp1049Gly
XM_011519024.1:c.3089A>G	XP_011517326.1:p.Asp1030Gly
XM_011519025.1:c.3065A>G	XP_011517327.1:p.Asp1022Gly
XM_011519026.1:c.3023A>G	XP_011517328.1:p.Asp1008Gly
XM_011519029.1:c.1589A>G	XP_011517331.1:p.Asp530Gly
XM_011519030.1:c.941A>G	XP_011517332.1:p.Asp314Gly
XM_011519031.1:c.728A>G	XP_011517333.1:p.Asp243Gly
XM_011519032.1:c.728A>G	XP_011517334.1:p.Asp243Gly
XM_011519033.1:c.3002A>G	XP_011517335.1:p.Asp1001Gly
NM_001354263.1:c.3137A>G	NP_001341192.1:p.Asp1046Gly
XM_005266105.5:c.3149A>G	XP_005266162.1:p.Asp1050Gly
XM_011519021.3:c.3167A>G	XP_011517323.1:p.Asp1056Gly
XM_011519022.3:c.3164A>G	XP_011517324.1:p.Asp1055Gly
XM_011519023.3:c.3146A>G	XP_011517325.1:p.Asp1049Gly
XM_011519029.3:c.1589A>G	XP_011517331.1:p.Asp530Gly
XM_011519030.3:c.941A>G	XP_011517332.1:p.Asp314Gly
XM_017015134.1:c.3143A>G	XP_016870623.1:p.Asp1048Gly
XM_017015136.2:c.3059A>G	XP_016870625.1:p.Asp1020Gly
XM_017015137.1:c.3044A>G	XP_016870626.1:p.Asp1015Gly
XM_017015138.1:c.3044A>G	XP_016870627.1:p.Asp1015Gly
XM_024447674.1:c.2987A>G	XP_024303442.1:p.Asp996Gly
XM_024447675.1:c.2921A>G	XP_024303443.1:p.Asp974Gly
XM_024447676.1:c.2282A>G	XP_024303444.1:p.Asp761Gly
XM_024447677.1:c.2282A>G	XP_024303445.1:p.Asp761Gly
XM_024447680.1:c.2900A>G	XP_024303448.1:p.Asp967Gly
NM_024757.5:c.3158A>G MANE Select	NP_079033.4:p.Asp1053Gly
NM_001354263.2:c.3137A>G	NP_001341192.1:p.Asp1046Gly