Canonical Allele Identifier: CA375794542

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707961C>G (hg19) ; chr9:g.137813509C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813509C>G , CM000671.2:g.137813509C>G	GRCh38
NC_000009.11:g.140707961C>G , CM000671.1:g.140707961C>G	GRCh37
NC_000009.10:g.139827782C>G	NCBI36
NG_011776.1:g.199518C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3159C>G MANE Select	ENSP00000417980.1:p.Asp1053Glu
ENST00000637161.1:c.3066C>G	ENSP00000490328.1:p.Asp1022Glu
ENST00000637261.1:c.3199C>G	ENSP00000490815.1:n.3199C>G
ENST00000637891.1:c.1053C>G	ENSP00000490907.1:p.Asp351Glu
ENST00000460843.5:c.3159C>G	ENSP00000417980.1:p.Asp1053Glu
ENST00000462942.3:c.2016C>G	ENSP00000436107.1:p.Asp672Glu
ENST00000483653.1:n.19C>G
ENST00000488242.2:n.685C>G
NM_024757.4:c.3159C>G	NP_079033.4:p.Asp1053Glu
XM_005266105.3:c.3150C>G	XP_005266162.1:p.Asp1050Glu
XM_005266110.1:c.3066C>G	XP_005266167.1:p.Asp1022Glu
XM_006717288.2:c.3141C>G	XP_006717351.1:p.Asp1047Glu
XM_011519021.1:c.3168C>G	XP_011517323.1:p.Asp1056Glu
XM_011519022.1:c.3165C>G	XP_011517324.1:p.Asp1055Glu
XM_011519023.1:c.3147C>G	XP_011517325.1:p.Asp1049Glu
XM_011519024.1:c.3090C>G	XP_011517326.1:p.Asp1030Glu
XM_011519025.1:c.3066C>G	XP_011517327.1:p.Asp1022Glu
XM_011519026.1:c.3024C>G	XP_011517328.1:p.Asp1008Glu
XM_011519029.1:c.1590C>G	XP_011517331.1:p.Asp530Glu
XM_011519030.1:c.942C>G	XP_011517332.1:p.Asp314Glu
XM_011519031.1:c.729C>G	XP_011517333.1:p.Asp243Glu
XM_011519032.1:c.729C>G	XP_011517334.1:p.Asp243Glu
XM_011519033.1:c.3003C>G	XP_011517335.1:p.Asp1001Glu
NM_001354263.1:c.3138C>G	NP_001341192.1:p.Asp1046Glu
XM_005266105.5:c.3150C>G	XP_005266162.1:p.Asp1050Glu
XM_011519021.3:c.3168C>G	XP_011517323.1:p.Asp1056Glu
XM_011519022.3:c.3165C>G	XP_011517324.1:p.Asp1055Glu
XM_011519023.3:c.3147C>G	XP_011517325.1:p.Asp1049Glu
XM_011519029.3:c.1590C>G	XP_011517331.1:p.Asp530Glu
XM_011519030.3:c.942C>G	XP_011517332.1:p.Asp314Glu
XM_017015134.1:c.3144C>G	XP_016870623.1:p.Asp1048Glu
XM_017015136.2:c.3060C>G	XP_016870625.1:p.Asp1020Glu
XM_017015137.1:c.3045C>G	XP_016870626.1:p.Asp1015Glu
XM_017015138.1:c.3045C>G	XP_016870627.1:p.Asp1015Glu
XM_024447674.1:c.2988C>G	XP_024303442.1:p.Asp996Glu
XM_024447675.1:c.2922C>G	XP_024303443.1:p.Asp974Glu
XM_024447676.1:c.2283C>G	XP_024303444.1:p.Asp761Glu
XM_024447677.1:c.2283C>G	XP_024303445.1:p.Asp761Glu
XM_024447680.1:c.2901C>G	XP_024303448.1:p.Asp967Glu
NM_024757.5:c.3159C>G MANE Select	NP_079033.4:p.Asp1053Glu
NM_001354263.2:c.3138C>G	NP_001341192.1:p.Asp1046Glu