Canonical Allele Identifier: CA375793893

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707860C>G (hg19) ; chr9:g.137813408C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813408C>G , CM000671.2:g.137813408C>G	GRCh38
NC_000009.11:g.140707860C>G , CM000671.1:g.140707860C>G	GRCh37
NC_000009.10:g.139827681C>G	NCBI36
NG_011776.1:g.199417C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3058C>G MANE Select	ENSP00000417980.1:p.Arg1020Gly
ENST00000636027.1:c.2944C>G
ENST00000637161.1:c.2965C>G	ENSP00000490328.1:p.Arg989Gly
ENST00000637261.1:c.3098C>G	ENSP00000490815.1:n.3098C>G
ENST00000637891.1:c.952C>G	ENSP00000490907.1:p.Arg318Gly
ENST00000460843.5:c.3058C>G	ENSP00000417980.1:p.Arg1020Gly
ENST00000462942.3:c.1915C>G	ENSP00000436107.1:p.Arg639Gly
ENST00000486164.5:c.745C>G
ENST00000488242.2:n.584C>G
NM_024757.4:c.3058C>G	NP_079033.4:p.Arg1020Gly
XM_005266105.3:c.3049C>G	XP_005266162.1:p.Arg1017Gly
XM_005266110.1:c.2965C>G	XP_005266167.1:p.Arg989Gly
XM_006717288.2:c.3040C>G	XP_006717351.1:p.Arg1014Gly
XM_011519021.1:c.3067C>G	XP_011517323.1:p.Arg1023Gly
XM_011519022.1:c.3064C>G	XP_011517324.1:p.Arg1022Gly
XM_011519023.1:c.3046C>G	XP_011517325.1:p.Arg1016Gly
XM_011519024.1:c.2989C>G	XP_011517326.1:p.Arg997Gly
XM_011519025.1:c.2965C>G	XP_011517327.1:p.Arg989Gly
XM_011519026.1:c.2923C>G	XP_011517328.1:p.Arg975Gly
XM_011519029.1:c.1489C>G	XP_011517331.1:p.Arg497Gly
XM_011519030.1:c.841C>G	XP_011517332.1:p.Arg281Gly
XM_011519031.1:c.628C>G	XP_011517333.1:p.Arg210Gly
XM_011519032.1:c.628C>G	XP_011517334.1:p.Arg210Gly
XM_011519033.1:c.2902C>G	XP_011517335.1:p.Arg968Gly
NM_001354263.1:c.3037C>G	NP_001341192.1:p.Arg1013Gly
XM_005266105.5:c.3049C>G	XP_005266162.1:p.Arg1017Gly
XM_011519021.3:c.3067C>G	XP_011517323.1:p.Arg1023Gly
XM_011519022.3:c.3064C>G	XP_011517324.1:p.Arg1022Gly
XM_011519023.3:c.3046C>G	XP_011517325.1:p.Arg1016Gly
XM_011519029.3:c.1489C>G	XP_011517331.1:p.Arg497Gly
XM_011519030.3:c.841C>G	XP_011517332.1:p.Arg281Gly
XM_017015134.1:c.3043C>G	XP_016870623.1:p.Arg1015Gly
XM_017015136.2:c.2959C>G	XP_016870625.1:p.Arg987Gly
XM_017015137.1:c.2944C>G	XP_016870626.1:p.Arg982Gly
XM_017015138.1:c.2944C>G	XP_016870627.1:p.Arg982Gly
XM_024447674.1:c.2887C>G	XP_024303442.1:p.Arg963Gly
XM_024447675.1:c.2821C>G	XP_024303443.1:p.Arg941Gly
XM_024447676.1:c.2182C>G	XP_024303444.1:p.Arg728Gly
XM_024447677.1:c.2182C>G	XP_024303445.1:p.Arg728Gly
XM_024447680.1:c.2800C>G	XP_024303448.1:p.Arg934Gly
NM_024757.5:c.3058C>G MANE Select	NP_079033.4:p.Arg1020Gly
NM_001354263.2:c.3037C>G	NP_001341192.1:p.Arg1013Gly