Canonical Allele Identifier: CA467874151

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671270G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776818G>A , CM000671.2:g.137776818G>A	GRCh38
NC_000009.11:g.140671270G>A , CM000671.1:g.140671270G>A	GRCh37
NC_000009.10:g.139791091G>A	NCBI36
NG_011776.1:g.162827G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1992G>A MANE Select	ENSP00000417980.1:p.Glu664=
ENST00000636027.1:c.1878G>A	ENSP00000489961.1:p.Glu626=
ENST00000637161.1:c.1899G>A	ENSP00000490328.1:p.Glu633=
ENST00000637261.1:c.2032G>A	ENSP00000490815.1:n.2032G>A
ENST00000638071.1:c.1619G>A
ENST00000640639.1:c.1161G>A	ENSP00000491823.1:p.Glu387=
ENST00000371394.6:c.*1727G>A	ENSP00000485945.1:n.*1727G>A
ENST00000460843.5:c.1992G>A	ENSP00000417980.1:p.Glu664=
ENST00000462484.5:c.1992G>A	ENSP00000417328.1:p.Glu664=
ENST00000462942.3:c.849G>A	ENSP00000436107.1:p.Glu283=
ENST00000626603.1:n.1631C>T
NM_001145527.1:c.1992G>A	NP_001138999.1:p.Glu664=
NM_024757.4:c.1992G>A	NP_079033.4:p.Glu664=
XM_005266105.3:c.1983G>A	XP_005266162.1:p.Glu661=
XM_005266110.1:c.1899G>A	XP_005266167.1:p.Glu633=
XM_006717288.2:c.1974G>A	XP_006717351.1:p.Glu658=
XM_011519021.1:c.2001G>A	XP_011517323.1:p.Glu667=
XM_011519022.1:c.1998G>A	XP_011517324.1:p.Glu666=
XM_011519023.1:c.1980G>A	XP_011517325.1:p.Glu660=
XM_011519024.1:c.1923G>A	XP_011517326.1:p.Glu641=
XM_011519025.1:c.1899G>A	XP_011517327.1:p.Glu633=
XM_011519026.1:c.1857G>A	XP_011517328.1:p.Glu619=
XM_011519027.1:c.2001G>A	XP_011517329.1:p.Glu667=
XM_011519028.1:c.2001G>A	XP_011517330.1:p.Glu667=
XM_011519029.1:c.423G>A	XP_011517331.1:p.Glu141=
XM_011519033.1:c.1836G>A	XP_011517335.1:p.Glu612=
NM_001354259.1:c.1899G>A	NP_001341188.1:p.Glu633=
NM_001354263.1:c.1971G>A	NP_001341192.1:p.Glu657=
XM_005266105.5:c.1983G>A	XP_005266162.1:p.Glu661=
XM_011519021.3:c.2001G>A	XP_011517323.1:p.Glu667=
XM_011519022.3:c.1998G>A	XP_011517324.1:p.Glu666=
XM_011519023.3:c.1980G>A	XP_011517325.1:p.Glu660=
XM_011519029.3:c.423G>A	XP_011517331.1:p.Glu141=
XM_017015134.1:c.1977G>A	XP_016870623.1:p.Glu659=
XM_017015136.2:c.1893G>A	XP_016870625.1:p.Glu631=
XM_017015137.1:c.1878G>A	XP_016870626.1:p.Glu626=
XM_017015138.1:c.1878G>A	XP_016870627.1:p.Glu626=
XM_024447674.1:c.1821G>A	XP_024303442.1:p.Glu607=
XM_024447675.1:c.1755G>A	XP_024303443.1:p.Glu585=
XM_024447676.1:c.1116G>A	XP_024303444.1:p.Glu372=
XM_024447677.1:c.1116G>A	XP_024303445.1:p.Glu372=
XM_024447678.1:c.1899G>A	XP_024303446.1:p.Glu633=
XM_024447679.1:c.1899G>A	XP_024303447.1:p.Glu633=
XM_024447680.1:c.1734G>A	XP_024303448.1:p.Glu578=
NM_024757.5:c.1992G>A MANE Select	NP_079033.4:p.Glu664=
NM_001145527.2:c.1992G>A	NP_001138999.1:p.Glu664=
NM_001354259.2:c.1899G>A	NP_001341188.1:p.Glu633=
NM_001354263.2:c.1971G>A	NP_001341192.1:p.Glu657=