Canonical Allele Identifier: CA467874157

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671279C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776827C>G , CM000671.2:g.137776827C>G	GRCh38
NC_000009.11:g.140671279C>G , CM000671.1:g.140671279C>G	GRCh37
NC_000009.10:g.139791100C>G	NCBI36
NG_011776.1:g.162836C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2001C>G MANE Select	ENSP00000417980.1:p.Ala667=
ENST00000636027.1:c.1887C>G	ENSP00000489961.1:p.Ala629=
ENST00000637161.1:c.1908C>G	ENSP00000490328.1:p.Ala636=
ENST00000637261.1:c.2041C>G	ENSP00000490815.1:n.2041C>G
ENST00000638071.1:c.1628C>G
ENST00000640639.1:c.1170C>G	ENSP00000491823.1:p.Ala390=
ENST00000371394.6:c.*1736C>G	ENSP00000485945.1:n.*1736C>G
ENST00000460843.5:c.2001C>G	ENSP00000417980.1:p.Ala667=
ENST00000462484.5:c.2001C>G	ENSP00000417328.1:p.Ala667=
ENST00000462942.3:c.858C>G	ENSP00000436107.1:p.Ala286=
ENST00000626603.1:n.1622G>C
NM_001145527.1:c.2001C>G	NP_001138999.1:p.Ala667=
NM_024757.4:c.2001C>G	NP_079033.4:p.Ala667=
XM_005266105.3:c.1992C>G	XP_005266162.1:p.Ala664=
XM_005266110.1:c.1908C>G	XP_005266167.1:p.Ala636=
XM_006717288.2:c.1983C>G	XP_006717351.1:p.Ala661=
XM_011519021.1:c.2010C>G	XP_011517323.1:p.Ala670=
XM_011519022.1:c.2007C>G	XP_011517324.1:p.Ala669=
XM_011519023.1:c.1989C>G	XP_011517325.1:p.Ala663=
XM_011519024.1:c.1932C>G	XP_011517326.1:p.Ala644=
XM_011519025.1:c.1908C>G	XP_011517327.1:p.Ala636=
XM_011519026.1:c.1866C>G	XP_011517328.1:p.Ala622=
XM_011519027.1:c.2010C>G	XP_011517329.1:p.Ala670=
XM_011519028.1:c.2010C>G	XP_011517330.1:p.Ala670=
XM_011519029.1:c.432C>G	XP_011517331.1:p.Ala144=
XM_011519033.1:c.1845C>G	XP_011517335.1:p.Ala615=
NM_001354259.1:c.1908C>G	NP_001341188.1:p.Ala636=
NM_001354263.1:c.1980C>G	NP_001341192.1:p.Ala660=
XM_005266105.5:c.1992C>G	XP_005266162.1:p.Ala664=
XM_011519021.3:c.2010C>G	XP_011517323.1:p.Ala670=
XM_011519022.3:c.2007C>G	XP_011517324.1:p.Ala669=
XM_011519023.3:c.1989C>G	XP_011517325.1:p.Ala663=
XM_011519029.3:c.432C>G	XP_011517331.1:p.Ala144=
XM_017015134.1:c.1986C>G	XP_016870623.1:p.Ala662=
XM_017015136.2:c.1902C>G	XP_016870625.1:p.Ala634=
XM_017015137.1:c.1887C>G	XP_016870626.1:p.Ala629=
XM_017015138.1:c.1887C>G	XP_016870627.1:p.Ala629=
XM_024447674.1:c.1830C>G	XP_024303442.1:p.Ala610=
XM_024447675.1:c.1764C>G	XP_024303443.1:p.Ala588=
XM_024447676.1:c.1125C>G	XP_024303444.1:p.Ala375=
XM_024447677.1:c.1125C>G	XP_024303445.1:p.Ala375=
XM_024447678.1:c.1908C>G	XP_024303446.1:p.Ala636=
XM_024447679.1:c.1908C>G	XP_024303447.1:p.Ala636=
XM_024447680.1:c.1743C>G	XP_024303448.1:p.Ala581=
NM_024757.5:c.2001C>G MANE Select	NP_079033.4:p.Ala667=
NM_001145527.2:c.2001C>G	NP_001138999.1:p.Ala667=
NM_001354259.2:c.1908C>G	NP_001341188.1:p.Ala636=
NM_001354263.2:c.1980C>G	NP_001341192.1:p.Ala660=