Canonical Allele Identifier: CA467874148

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671267G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776815G>A , CM000671.2:g.137776815G>A	GRCh38
NC_000009.11:g.140671267G>A , CM000671.1:g.140671267G>A	GRCh37
NC_000009.10:g.139791088G>A	NCBI36
NG_011776.1:g.162824G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1989G>A MANE Select	ENSP00000417980.1:p.Leu663=
ENST00000636027.1:c.1875G>A	ENSP00000489961.1:p.Leu625=
ENST00000637161.1:c.1896G>A	ENSP00000490328.1:p.Leu632=
ENST00000637261.1:c.2029G>A	ENSP00000490815.1:n.2029G>A
ENST00000638071.1:c.1616G>A
ENST00000640639.1:c.1158G>A	ENSP00000491823.1:p.Leu386=
ENST00000371394.6:c.*1724G>A	ENSP00000485945.1:n.*1724G>A
ENST00000460843.5:c.1989G>A	ENSP00000417980.1:p.Leu663=
ENST00000462484.5:c.1989G>A	ENSP00000417328.1:p.Leu663=
ENST00000462942.3:c.846G>A	ENSP00000436107.1:p.Leu282=
ENST00000626603.1:n.1634C>T
NM_001145527.1:c.1989G>A	NP_001138999.1:p.Leu663=
NM_024757.4:c.1989G>A	NP_079033.4:p.Leu663=
XM_005266105.3:c.1980G>A	XP_005266162.1:p.Leu660=
XM_005266110.1:c.1896G>A	XP_005266167.1:p.Leu632=
XM_006717288.2:c.1971G>A	XP_006717351.1:p.Leu657=
XM_011519021.1:c.1998G>A	XP_011517323.1:p.Leu666=
XM_011519022.1:c.1995G>A	XP_011517324.1:p.Leu665=
XM_011519023.1:c.1977G>A	XP_011517325.1:p.Leu659=
XM_011519024.1:c.1920G>A	XP_011517326.1:p.Leu640=
XM_011519025.1:c.1896G>A	XP_011517327.1:p.Leu632=
XM_011519026.1:c.1854G>A	XP_011517328.1:p.Leu618=
XM_011519027.1:c.1998G>A	XP_011517329.1:p.Leu666=
XM_011519028.1:c.1998G>A	XP_011517330.1:p.Leu666=
XM_011519029.1:c.420G>A	XP_011517331.1:p.Leu140=
XM_011519033.1:c.1833G>A	XP_011517335.1:p.Leu611=
NM_001354259.1:c.1896G>A	NP_001341188.1:p.Leu632=
NM_001354263.1:c.1968G>A	NP_001341192.1:p.Leu656=
XM_005266105.5:c.1980G>A	XP_005266162.1:p.Leu660=
XM_011519021.3:c.1998G>A	XP_011517323.1:p.Leu666=
XM_011519022.3:c.1995G>A	XP_011517324.1:p.Leu665=
XM_011519023.3:c.1977G>A	XP_011517325.1:p.Leu659=
XM_011519029.3:c.420G>A	XP_011517331.1:p.Leu140=
XM_017015134.1:c.1974G>A	XP_016870623.1:p.Leu658=
XM_017015136.2:c.1890G>A	XP_016870625.1:p.Leu630=
XM_017015137.1:c.1875G>A	XP_016870626.1:p.Leu625=
XM_017015138.1:c.1875G>A	XP_016870627.1:p.Leu625=
XM_024447674.1:c.1818G>A	XP_024303442.1:p.Leu606=
XM_024447675.1:c.1752G>A	XP_024303443.1:p.Leu584=
XM_024447676.1:c.1113G>A	XP_024303444.1:p.Leu371=
XM_024447677.1:c.1113G>A	XP_024303445.1:p.Leu371=
XM_024447678.1:c.1896G>A	XP_024303446.1:p.Leu632=
XM_024447679.1:c.1896G>A	XP_024303447.1:p.Leu632=
XM_024447680.1:c.1731G>A	XP_024303448.1:p.Leu577=
NM_024757.5:c.1989G>A MANE Select	NP_079033.4:p.Leu663=
NM_001145527.2:c.1989G>A	NP_001138999.1:p.Leu663=
NM_001354259.2:c.1896G>A	NP_001341188.1:p.Leu632=
NM_001354263.2:c.1968G>A	NP_001341192.1:p.Leu656=