Canonical Allele Identifier: CA467874114

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671219C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776767C>G , CM000671.2:g.137776767C>G	GRCh38
NC_000009.11:g.140671219C>G , CM000671.1:g.140671219C>G	GRCh37
NC_000009.10:g.139791040C>G	NCBI36
NG_011776.1:g.162776C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1941C>G MANE Select	ENSP00000417980.1:p.Thr647=
ENST00000636027.1:c.1827C>G	ENSP00000489961.1:p.Thr609=
ENST00000637161.1:c.1848C>G	ENSP00000490328.1:p.Thr616=
ENST00000637261.1:c.1981C>G	ENSP00000490815.1:n.1981C>G
ENST00000638071.1:c.1568C>G
ENST00000640639.1:c.1110C>G	ENSP00000491823.1:p.Thr370=
ENST00000371394.6:c.*1676C>G	ENSP00000485945.1:n.*1676C>G
ENST00000460843.5:c.1941C>G	ENSP00000417980.1:p.Thr647=
ENST00000462484.5:c.1941C>G	ENSP00000417328.1:p.Thr647=
ENST00000462942.3:c.798C>G	ENSP00000436107.1:p.Thr266=
ENST00000465566.2:c.489C>G	ENSP00000486261.1:p.Thr163=
ENST00000626603.1:n.1682G>C
NM_001145527.1:c.1941C>G	NP_001138999.1:p.Thr647=
NM_024757.4:c.1941C>G	NP_079033.4:p.Thr647=
XM_005266105.3:c.1932C>G	XP_005266162.1:p.Thr644=
XM_005266110.1:c.1848C>G	XP_005266167.1:p.Thr616=
XM_006717288.2:c.1923C>G	XP_006717351.1:p.Thr641=
XM_011519021.1:c.1950C>G	XP_011517323.1:p.Thr650=
XM_011519022.1:c.1947C>G	XP_011517324.1:p.Thr649=
XM_011519023.1:c.1929C>G	XP_011517325.1:p.Thr643=
XM_011519024.1:c.1872C>G	XP_011517326.1:p.Thr624=
XM_011519025.1:c.1848C>G	XP_011517327.1:p.Thr616=
XM_011519026.1:c.1806C>G	XP_011517328.1:p.Thr602=
XM_011519027.1:c.1950C>G	XP_011517329.1:p.Thr650=
XM_011519028.1:c.1950C>G	XP_011517330.1:p.Thr650=
XM_011519029.1:c.372C>G	XP_011517331.1:p.Thr124=
XM_011519033.1:c.1785C>G	XP_011517335.1:p.Thr595=
NM_001354259.1:c.1848C>G	NP_001341188.1:p.Thr616=
NM_001354263.1:c.1920C>G	NP_001341192.1:p.Thr640=
XM_005266105.5:c.1932C>G	XP_005266162.1:p.Thr644=
XM_011519021.3:c.1950C>G	XP_011517323.1:p.Thr650=
XM_011519022.3:c.1947C>G	XP_011517324.1:p.Thr649=
XM_011519023.3:c.1929C>G	XP_011517325.1:p.Thr643=
XM_011519029.3:c.372C>G	XP_011517331.1:p.Thr124=
XM_017015134.1:c.1926C>G	XP_016870623.1:p.Thr642=
XM_017015136.2:c.1842C>G	XP_016870625.1:p.Thr614=
XM_017015137.1:c.1827C>G	XP_016870626.1:p.Thr609=
XM_017015138.1:c.1827C>G	XP_016870627.1:p.Thr609=
XM_024447674.1:c.1770C>G	XP_024303442.1:p.Thr590=
XM_024447675.1:c.1704C>G	XP_024303443.1:p.Thr568=
XM_024447676.1:c.1065C>G	XP_024303444.1:p.Thr355=
XM_024447677.1:c.1065C>G	XP_024303445.1:p.Thr355=
XM_024447678.1:c.1848C>G	XP_024303446.1:p.Thr616=
XM_024447679.1:c.1848C>G	XP_024303447.1:p.Thr616=
XM_024447680.1:c.1683C>G	XP_024303448.1:p.Thr561=
NM_024757.5:c.1941C>G MANE Select	NP_079033.4:p.Thr647=
NM_001145527.2:c.1941C>G	NP_001138999.1:p.Thr647=
NM_001354259.2:c.1848C>G	NP_001341188.1:p.Thr616=
NM_001354263.2:c.1920C>G	NP_001341192.1:p.Thr640=