Canonical Allele Identifier: CA468161063

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707539T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813087T>G , CM000671.2:g.137813087T>G	GRCh38
NC_000009.11:g.140707539T>G , CM000671.1:g.140707539T>G	GRCh37
NC_000009.10:g.139827360T>G	NCBI36
NG_011776.1:g.199096T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2949T>G MANE Select	ENSP00000417980.1:p.Ser983=
ENST00000636027.1:c.2835T>G	ENSP00000489961.1:p.Ser945=
ENST00000637161.1:c.2856T>G	ENSP00000490328.1:p.Ser952=
ENST00000637261.1:c.2989T>G	ENSP00000490815.1:n.2989T>G
ENST00000637891.1:c.843T>G	ENSP00000490907.1:p.Ser281=
ENST00000460843.5:c.2949T>G	ENSP00000417980.1:p.Ser983=
ENST00000462942.3:c.1806T>G	ENSP00000436107.1:p.Ser602=
ENST00000486164.5:c.636T>G
ENST00000488242.2:n.475T>G
NM_024757.4:c.2949T>G	NP_079033.4:p.Ser983=
XM_005266105.3:c.2940T>G	XP_005266162.1:p.Ser980=
XM_005266110.1:c.2856T>G	XP_005266167.1:p.Ser952=
XM_006717288.2:c.2931T>G	XP_006717351.1:p.Ser977=
XM_011519021.1:c.2958T>G	XP_011517323.1:p.Ser986=
XM_011519022.1:c.2955T>G	XP_011517324.1:p.Ser985=
XM_011519023.1:c.2937T>G	XP_011517325.1:p.Ser979=
XM_011519024.1:c.2880T>G	XP_011517326.1:p.Ser960=
XM_011519025.1:c.2856T>G	XP_011517327.1:p.Ser952=
XM_011519026.1:c.2814T>G	XP_011517328.1:p.Ser938=
XM_011519029.1:c.1380T>G	XP_011517331.1:p.Ser460=
XM_011519030.1:c.732T>G	XP_011517332.1:p.Ser244=
XM_011519031.1:c.519T>G	XP_011517333.1:p.Ser173=
XM_011519032.1:c.519T>G	XP_011517334.1:p.Ser173=
XM_011519033.1:c.2793T>G	XP_011517335.1:p.Ser931=
NM_001354263.1:c.2928T>G	NP_001341192.1:p.Ser976=
XM_005266105.5:c.2940T>G	XP_005266162.1:p.Ser980=
XM_011519021.3:c.2958T>G	XP_011517323.1:p.Ser986=
XM_011519022.3:c.2955T>G	XP_011517324.1:p.Ser985=
XM_011519023.3:c.2937T>G	XP_011517325.1:p.Ser979=
XM_011519029.3:c.1380T>G	XP_011517331.1:p.Ser460=
XM_011519030.3:c.732T>G	XP_011517332.1:p.Ser244=
XM_017015134.1:c.2934T>G	XP_016870623.1:p.Ser978=
XM_017015136.2:c.2850T>G	XP_016870625.1:p.Ser950=
XM_017015137.1:c.2835T>G	XP_016870626.1:p.Ser945=
XM_017015138.1:c.2835T>G	XP_016870627.1:p.Ser945=
XM_024447674.1:c.2778T>G	XP_024303442.1:p.Ser926=
XM_024447675.1:c.2712T>G	XP_024303443.1:p.Ser904=
XM_024447676.1:c.2073T>G	XP_024303444.1:p.Ser691=
XM_024447677.1:c.2073T>G	XP_024303445.1:p.Ser691=
XM_024447680.1:c.2691T>G	XP_024303448.1:p.Ser897=
NM_024757.5:c.2949T>G MANE Select	NP_079033.4:p.Ser983=
NM_001354263.2:c.2928T>G	NP_001341192.1:p.Ser976=