Canonical Allele Identifier: CA375775673

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671095A>G (hg19) ; chr9:g.137776643A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776643A>G , CM000671.2:g.137776643A>G	GRCh38
NC_000009.11:g.140671095A>G , CM000671.1:g.140671095A>G	GRCh37
NC_000009.10:g.139790916A>G	NCBI36
NG_011776.1:g.162652A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.1817A>G MANE Select	ENSP00000417980.1:p.Glu606Gly
ENST00000636027.1:c.1703A>G	ENSP00000489961.1:p.Glu568Gly
ENST00000637161.1:c.1724A>G	ENSP00000490328.1:p.Glu575Gly
ENST00000637261.1:c.1857A>G	ENSP00000490815.1:n.1857A>G
ENST00000638071.1:c.1444A>G
ENST00000640639.1:c.986A>G	ENSP00000491823.1:p.Glu329Gly
ENST00000371394.6:c.*1552A>G	ENSP00000485945.1:n.*1552A>G
ENST00000460843.5:c.1817A>G	ENSP00000417980.1:p.Glu606Gly
ENST00000462484.5:c.1817A>G	ENSP00000417328.1:p.Glu606Gly
ENST00000462942.3:c.674A>G	ENSP00000436107.1:p.Glu225Gly
ENST00000465566.2:c.365A>G	ENSP00000486261.1:p.Glu122Gly
ENST00000626603.1:n.1806T>C
NM_001145527.1:c.1817A>G	NP_001138999.1:p.Glu606Gly
NM_024757.4:c.1817A>G	NP_079033.4:p.Glu606Gly
XM_005266105.3:c.1808A>G	XP_005266162.1:p.Glu603Gly
XM_005266110.1:c.1724A>G	XP_005266167.1:p.Glu575Gly
XM_006717288.2:c.1799A>G	XP_006717351.1:p.Glu600Gly
XM_011519021.1:c.1826A>G	XP_011517323.1:p.Glu609Gly
XM_011519022.1:c.1823A>G	XP_011517324.1:p.Glu608Gly
XM_011519023.1:c.1805A>G	XP_011517325.1:p.Glu602Gly
XM_011519024.1:c.1748A>G	XP_011517326.1:p.Glu583Gly
XM_011519025.1:c.1724A>G	XP_011517327.1:p.Glu575Gly
XM_011519026.1:c.1682A>G	XP_011517328.1:p.Glu561Gly
XM_011519027.1:c.1826A>G	XP_011517329.1:p.Glu609Gly
XM_011519028.1:c.1826A>G	XP_011517330.1:p.Glu609Gly
XM_011519029.1:c.248A>G	XP_011517331.1:p.Glu83Gly
XM_011519033.1:c.1661A>G	XP_011517335.1:p.Glu554Gly
NM_001354259.1:c.1724A>G	NP_001341188.1:p.Glu575Gly
NM_001354263.1:c.1796A>G	NP_001341192.1:p.Glu599Gly
XM_005266105.5:c.1808A>G	XP_005266162.1:p.Glu603Gly
XM_011519021.3:c.1826A>G	XP_011517323.1:p.Glu609Gly
XM_011519022.3:c.1823A>G	XP_011517324.1:p.Glu608Gly
XM_011519023.3:c.1805A>G	XP_011517325.1:p.Glu602Gly
XM_011519029.3:c.248A>G	XP_011517331.1:p.Glu83Gly
XM_017015134.1:c.1802A>G	XP_016870623.1:p.Glu601Gly
XM_017015136.2:c.1718A>G	XP_016870625.1:p.Glu573Gly
XM_017015137.1:c.1703A>G	XP_016870626.1:p.Glu568Gly
XM_017015138.1:c.1703A>G	XP_016870627.1:p.Glu568Gly
XM_024447674.1:c.1646A>G	XP_024303442.1:p.Glu549Gly
XM_024447675.1:c.1580A>G	XP_024303443.1:p.Glu527Gly
XM_024447676.1:c.941A>G	XP_024303444.1:p.Glu314Gly
XM_024447677.1:c.941A>G	XP_024303445.1:p.Glu314Gly
XM_024447678.1:c.1724A>G	XP_024303446.1:p.Glu575Gly
XM_024447679.1:c.1724A>G	XP_024303447.1:p.Glu575Gly
XM_024447680.1:c.1559A>G	XP_024303448.1:p.Glu520Gly
NM_024757.5:c.1817A>G MANE Select	NP_079033.4:p.Glu606Gly
NM_001145527.2:c.1817A>G	NP_001138999.1:p.Glu606Gly
NM_001354259.2:c.1724A>G	NP_001341188.1:p.Glu575Gly
NM_001354263.2:c.1796A>G	NP_001341192.1:p.Glu599Gly