Canonical Allele Identifier: CA467874087

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137776722-G-A
• MyVariant Identifiers: chr9:g.140671174G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776722G>A , CM000671.2:g.137776722G>A	GRCh38
NC_000009.11:g.140671174G>A , CM000671.1:g.140671174G>A	GRCh37
NC_000009.10:g.139790995G>A	NCBI36
NG_011776.1:g.162731G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1896G>A MANE Select	ENSP00000417980.1:p.Glu632=
ENST00000636027.1:c.1782G>A	ENSP00000489961.1:p.Glu594=
ENST00000637161.1:c.1803G>A	ENSP00000490328.1:p.Glu601=
ENST00000637261.1:c.1936G>A	ENSP00000490815.1:n.1936G>A
ENST00000638071.1:c.1523G>A
ENST00000640639.1:c.1065G>A	ENSP00000491823.1:p.Glu355=
ENST00000371394.6:c.*1631G>A	ENSP00000485945.1:n.*1631G>A
ENST00000460843.5:c.1896G>A	ENSP00000417980.1:p.Glu632=
ENST00000462484.5:c.1896G>A	ENSP00000417328.1:p.Glu632=
ENST00000462942.3:c.753G>A	ENSP00000436107.1:p.Glu251=
ENST00000465566.2:c.444G>A	ENSP00000486261.1:p.Glu148=
ENST00000626603.1:n.1727C>T
NM_001145527.1:c.1896G>A	NP_001138999.1:p.Glu632=
NM_024757.4:c.1896G>A	NP_079033.4:p.Glu632=
XM_005266105.3:c.1887G>A	XP_005266162.1:p.Glu629=
XM_005266110.1:c.1803G>A	XP_005266167.1:p.Glu601=
XM_006717288.2:c.1878G>A	XP_006717351.1:p.Glu626=
XM_011519021.1:c.1905G>A	XP_011517323.1:p.Glu635=
XM_011519022.1:c.1902G>A	XP_011517324.1:p.Glu634=
XM_011519023.1:c.1884G>A	XP_011517325.1:p.Glu628=
XM_011519024.1:c.1827G>A	XP_011517326.1:p.Glu609=
XM_011519025.1:c.1803G>A	XP_011517327.1:p.Glu601=
XM_011519026.1:c.1761G>A	XP_011517328.1:p.Glu587=
XM_011519027.1:c.1905G>A	XP_011517329.1:p.Glu635=
XM_011519028.1:c.1905G>A	XP_011517330.1:p.Glu635=
XM_011519029.1:c.327G>A	XP_011517331.1:p.Glu109=
XM_011519033.1:c.1740G>A	XP_011517335.1:p.Glu580=
NM_001354259.1:c.1803G>A	NP_001341188.1:p.Glu601=
NM_001354263.1:c.1875G>A	NP_001341192.1:p.Glu625=
XM_005266105.5:c.1887G>A	XP_005266162.1:p.Glu629=
XM_011519021.3:c.1905G>A	XP_011517323.1:p.Glu635=
XM_011519022.3:c.1902G>A	XP_011517324.1:p.Glu634=
XM_011519023.3:c.1884G>A	XP_011517325.1:p.Glu628=
XM_011519029.3:c.327G>A	XP_011517331.1:p.Glu109=
XM_017015134.1:c.1881G>A	XP_016870623.1:p.Glu627=
XM_017015136.2:c.1797G>A	XP_016870625.1:p.Glu599=
XM_017015137.1:c.1782G>A	XP_016870626.1:p.Glu594=
XM_017015138.1:c.1782G>A	XP_016870627.1:p.Glu594=
XM_024447674.1:c.1725G>A	XP_024303442.1:p.Glu575=
XM_024447675.1:c.1659G>A	XP_024303443.1:p.Glu553=
XM_024447676.1:c.1020G>A	XP_024303444.1:p.Glu340=
XM_024447677.1:c.1020G>A	XP_024303445.1:p.Glu340=
XM_024447678.1:c.1803G>A	XP_024303446.1:p.Glu601=
XM_024447679.1:c.1803G>A	XP_024303447.1:p.Glu601=
XM_024447680.1:c.1638G>A	XP_024303448.1:p.Glu546=
NM_024757.5:c.1896G>A MANE Select	NP_079033.4:p.Glu632=
NM_001145527.2:c.1896G>A	NP_001138999.1:p.Glu632=
NM_001354259.2:c.1803G>A	NP_001341188.1:p.Glu601=
NM_001354263.2:c.1875G>A	NP_001341192.1:p.Glu625=