Canonical Allele Identifier: CA375793426

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707528A>G (hg19) ; chr9:g.137813076A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813076A>G , CM000671.2:g.137813076A>G	GRCh38
NC_000009.11:g.140707528A>G , CM000671.1:g.140707528A>G	GRCh37
NC_000009.10:g.139827349A>G	NCBI36
NG_011776.1:g.199085A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2938A>G MANE Select	ENSP00000417980.1:p.Ser980Gly
ENST00000636027.1:c.2824A>G	ENSP00000489961.1:p.Ser942Gly
ENST00000637161.1:c.2845A>G	ENSP00000490328.1:p.Ser949Gly
ENST00000637261.1:c.2978A>G	ENSP00000490815.1:n.2978A>G
ENST00000637891.1:c.832A>G	ENSP00000490907.1:p.Ser278Gly
ENST00000460843.5:c.2938A>G	ENSP00000417980.1:p.Ser980Gly
ENST00000462942.3:c.1795A>G	ENSP00000436107.1:p.Ser599Gly
ENST00000486164.5:c.625A>G
ENST00000488242.2:n.464A>G
NM_024757.4:c.2938A>G	NP_079033.4:p.Ser980Gly
XM_005266105.3:c.2929A>G	XP_005266162.1:p.Ser977Gly
XM_005266110.1:c.2845A>G	XP_005266167.1:p.Ser949Gly
XM_006717288.2:c.2920A>G	XP_006717351.1:p.Ser974Gly
XM_011519021.1:c.2947A>G	XP_011517323.1:p.Ser983Gly
XM_011519022.1:c.2944A>G	XP_011517324.1:p.Ser982Gly
XM_011519023.1:c.2926A>G	XP_011517325.1:p.Ser976Gly
XM_011519024.1:c.2869A>G	XP_011517326.1:p.Ser957Gly
XM_011519025.1:c.2845A>G	XP_011517327.1:p.Ser949Gly
XM_011519026.1:c.2803A>G	XP_011517328.1:p.Ser935Gly
XM_011519029.1:c.1369A>G	XP_011517331.1:p.Ser457Gly
XM_011519030.1:c.721A>G	XP_011517332.1:p.Ser241Gly
XM_011519031.1:c.508A>G	XP_011517333.1:p.Ser170Gly
XM_011519032.1:c.508A>G	XP_011517334.1:p.Ser170Gly
XM_011519033.1:c.2782A>G	XP_011517335.1:p.Ser928Gly
NM_001354263.1:c.2917A>G	NP_001341192.1:p.Ser973Gly
XM_005266105.5:c.2929A>G	XP_005266162.1:p.Ser977Gly
XM_011519021.3:c.2947A>G	XP_011517323.1:p.Ser983Gly
XM_011519022.3:c.2944A>G	XP_011517324.1:p.Ser982Gly
XM_011519023.3:c.2926A>G	XP_011517325.1:p.Ser976Gly
XM_011519029.3:c.1369A>G	XP_011517331.1:p.Ser457Gly
XM_011519030.3:c.721A>G	XP_011517332.1:p.Ser241Gly
XM_017015134.1:c.2923A>G	XP_016870623.1:p.Ser975Gly
XM_017015136.2:c.2839A>G	XP_016870625.1:p.Ser947Gly
XM_017015137.1:c.2824A>G	XP_016870626.1:p.Ser942Gly
XM_017015138.1:c.2824A>G	XP_016870627.1:p.Ser942Gly
XM_024447674.1:c.2767A>G	XP_024303442.1:p.Ser923Gly
XM_024447675.1:c.2701A>G	XP_024303443.1:p.Ser901Gly
XM_024447676.1:c.2062A>G	XP_024303444.1:p.Ser688Gly
XM_024447677.1:c.2062A>G	XP_024303445.1:p.Ser688Gly
XM_024447680.1:c.2680A>G	XP_024303448.1:p.Ser894Gly
NM_024757.5:c.2938A>G MANE Select	NP_079033.4:p.Ser980Gly
NM_001354263.2:c.2917A>G	NP_001341192.1:p.Ser973Gly