Canonical Allele Identifier: CA467874164

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671288A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776836A>C , CM000671.2:g.137776836A>C	GRCh38
NC_000009.11:g.140671288A>C , CM000671.1:g.140671288A>C	GRCh37
NC_000009.10:g.139791109A>C	NCBI36
NG_011776.1:g.162845A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2010A>C MANE Select	ENSP00000417980.1:p.Thr670=
ENST00000636027.1:c.1896A>C	ENSP00000489961.1:p.Thr632=
ENST00000637161.1:c.1917A>C	ENSP00000490328.1:p.Thr639=
ENST00000637261.1:c.2050A>C	ENSP00000490815.1:n.2050A>C
ENST00000638071.1:c.1637A>C
ENST00000640639.1:c.1179A>C	ENSP00000491823.1:p.Thr393=
ENST00000371394.6:c.*1745A>C	ENSP00000485945.1:n.*1745A>C
ENST00000460843.5:c.2010A>C	ENSP00000417980.1:p.Thr670=
ENST00000462484.5:c.2010A>C	ENSP00000417328.1:p.Thr670=
ENST00000462942.3:c.867A>C	ENSP00000436107.1:p.Thr289=
ENST00000626603.1:n.1613T>G
NM_001145527.1:c.2010A>C	NP_001138999.1:p.Thr670=
NM_024757.4:c.2010A>C	NP_079033.4:p.Thr670=
XM_005266105.3:c.2001A>C	XP_005266162.1:p.Thr667=
XM_005266110.1:c.1917A>C	XP_005266167.1:p.Thr639=
XM_006717288.2:c.1992A>C	XP_006717351.1:p.Thr664=
XM_011519021.1:c.2019A>C	XP_011517323.1:p.Thr673=
XM_011519022.1:c.2016A>C	XP_011517324.1:p.Thr672=
XM_011519023.1:c.1998A>C	XP_011517325.1:p.Thr666=
XM_011519024.1:c.1941A>C	XP_011517326.1:p.Thr647=
XM_011519025.1:c.1917A>C	XP_011517327.1:p.Thr639=
XM_011519026.1:c.1875A>C	XP_011517328.1:p.Thr625=
XM_011519027.1:c.2019A>C	XP_011517329.1:p.Thr673=
XM_011519028.1:c.2019A>C	XP_011517330.1:p.Thr673=
XM_011519029.1:c.441A>C	XP_011517331.1:p.Thr147=
XM_011519033.1:c.1854A>C	XP_011517335.1:p.Thr618=
NM_001354259.1:c.1917A>C	NP_001341188.1:p.Thr639=
NM_001354263.1:c.1989A>C	NP_001341192.1:p.Thr663=
XM_005266105.5:c.2001A>C	XP_005266162.1:p.Thr667=
XM_011519021.3:c.2019A>C	XP_011517323.1:p.Thr673=
XM_011519022.3:c.2016A>C	XP_011517324.1:p.Thr672=
XM_011519023.3:c.1998A>C	XP_011517325.1:p.Thr666=
XM_011519029.3:c.441A>C	XP_011517331.1:p.Thr147=
XM_017015134.1:c.1995A>C	XP_016870623.1:p.Thr665=
XM_017015136.2:c.1911A>C	XP_016870625.1:p.Thr637=
XM_017015137.1:c.1896A>C	XP_016870626.1:p.Thr632=
XM_017015138.1:c.1896A>C	XP_016870627.1:p.Thr632=
XM_024447674.1:c.1839A>C	XP_024303442.1:p.Thr613=
XM_024447675.1:c.1773A>C	XP_024303443.1:p.Thr591=
XM_024447676.1:c.1134A>C	XP_024303444.1:p.Thr378=
XM_024447677.1:c.1134A>C	XP_024303445.1:p.Thr378=
XM_024447678.1:c.1917A>C	XP_024303446.1:p.Thr639=
XM_024447679.1:c.1917A>C	XP_024303447.1:p.Thr639=
XM_024447680.1:c.1752A>C	XP_024303448.1:p.Thr584=
NM_024757.5:c.2010A>C MANE Select	NP_079033.4:p.Thr670=
NM_001145527.2:c.2010A>C	NP_001138999.1:p.Thr670=
NM_001354259.2:c.1917A>C	NP_001341188.1:p.Thr639=
NM_001354263.2:c.1989A>C	NP_001341192.1:p.Thr663=