Canonical Allele Identifier: CA375793203

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707469C>G (hg19) ; chr9:g.137813017C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813017C>G , CM000671.2:g.137813017C>G	GRCh38
NC_000009.11:g.140707469C>G , CM000671.1:g.140707469C>G	GRCh37
NC_000009.10:g.139827290C>G	NCBI36
NG_011776.1:g.199026C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2879C>G MANE Select	ENSP00000417980.1:p.Ser960Cys
ENST00000636027.1:c.2765C>G	ENSP00000489961.1:p.Ser922Cys
ENST00000637161.1:c.2786C>G	ENSP00000490328.1:p.Ser929Cys
ENST00000637261.1:c.2919C>G	ENSP00000490815.1:n.2919C>G
ENST00000637891.1:c.773C>G	ENSP00000490907.1:p.Ser258Cys
ENST00000460843.5:c.2879C>G	ENSP00000417980.1:p.Ser960Cys
ENST00000462942.3:c.1736C>G	ENSP00000436107.1:p.Ser579Cys
ENST00000486164.5:c.566C>G
ENST00000488242.2:n.405C>G
NM_024757.4:c.2879C>G	NP_079033.4:p.Ser960Cys
XM_005266105.3:c.2870C>G	XP_005266162.1:p.Ser957Cys
XM_005266110.1:c.2786C>G	XP_005266167.1:p.Ser929Cys
XM_006717288.2:c.2861C>G	XP_006717351.1:p.Ser954Cys
XM_011519021.1:c.2888C>G	XP_011517323.1:p.Ser963Cys
XM_011519022.1:c.2885C>G	XP_011517324.1:p.Ser962Cys
XM_011519023.1:c.2867C>G	XP_011517325.1:p.Ser956Cys
XM_011519024.1:c.2810C>G	XP_011517326.1:p.Ser937Cys
XM_011519025.1:c.2786C>G	XP_011517327.1:p.Ser929Cys
XM_011519026.1:c.2744C>G	XP_011517328.1:p.Ser915Cys
XM_011519029.1:c.1310C>G	XP_011517331.1:p.Ser437Cys
XM_011519030.1:c.662C>G	XP_011517332.1:p.Ser221Cys
XM_011519031.1:c.449C>G	XP_011517333.1:p.Ser150Cys
XM_011519032.1:c.449C>G	XP_011517334.1:p.Ser150Cys
XM_011519033.1:c.2723C>G	XP_011517335.1:p.Ser908Cys
NM_001354263.1:c.2858C>G	NP_001341192.1:p.Ser953Cys
XM_005266105.5:c.2870C>G	XP_005266162.1:p.Ser957Cys
XM_011519021.3:c.2888C>G	XP_011517323.1:p.Ser963Cys
XM_011519022.3:c.2885C>G	XP_011517324.1:p.Ser962Cys
XM_011519023.3:c.2867C>G	XP_011517325.1:p.Ser956Cys
XM_011519029.3:c.1310C>G	XP_011517331.1:p.Ser437Cys
XM_011519030.3:c.662C>G	XP_011517332.1:p.Ser221Cys
XM_017015134.1:c.2864C>G	XP_016870623.1:p.Ser955Cys
XM_017015136.2:c.2780C>G	XP_016870625.1:p.Ser927Cys
XM_017015137.1:c.2765C>G	XP_016870626.1:p.Ser922Cys
XM_017015138.1:c.2765C>G	XP_016870627.1:p.Ser922Cys
XM_024447674.1:c.2708C>G	XP_024303442.1:p.Ser903Cys
XM_024447675.1:c.2642C>G	XP_024303443.1:p.Ser881Cys
XM_024447676.1:c.2003C>G	XP_024303444.1:p.Ser668Cys
XM_024447677.1:c.2003C>G	XP_024303445.1:p.Ser668Cys
XM_024447680.1:c.2621C>G	XP_024303448.1:p.Ser874Cys
NM_024757.5:c.2879C>G MANE Select	NP_079033.4:p.Ser960Cys
NM_001354263.2:c.2858C>G	NP_001341192.1:p.Ser953Cys