Canonical Allele Identifier: CA1884659568

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137762719G= , CM000671.2:g.137762719G=	GRCh38
NC_000009.11:g.140657171G= , CM000671.1:g.140657171G=	GRCh37
NC_000009.10:g.139776992G=	NCBI36
NG_011776.1:g.148728G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1546G= MANE Select	ENSP00000417980.1:p.Glu516=
ENST00000629335.2:c.1546G=	ENSP00000490056.1:p.Glu516=
ENST00000636027.1:c.1432G=	ENSP00000489961.1:p.Glu478=
ENST00000637161.1:c.1453G=	ENSP00000490328.1:p.Glu485=
ENST00000637261.1:c.1586G=	ENSP00000490815.1:n.1586G=
ENST00000637977.1:c.1491G=
ENST00000638071.1:c.1173G=
ENST00000640639.1:c.715G=	ENSP00000491823.1:p.Glu239=
ENST00000371394.6:c.*1281G=	ENSP00000485945.1:n.*1281G=
ENST00000460843.5:c.1546G=	ENSP00000417980.1:p.Glu516=
ENST00000462484.5:c.1546G=	ENSP00000417328.1:p.Glu516=
ENST00000462942.3:c.403G=	ENSP00000436107.1:p.Glu135=
ENST00000465566.2:c.238G=	ENSP00000486261.1:p.Glu80=
ENST00000629808.2:c.639G=
NM_001145527.1:c.1546G=	NP_001138999.1:p.Glu516=
NM_024757.4:c.1546G=	NP_079033.4:p.Glu516=
XM_005266105.3:c.1537G=	XP_005266162.1:p.Glu513=
XM_005266110.1:c.1453G=	XP_005266167.1:p.Glu485=
XM_006717288.2:c.1528G=	XP_006717351.1:p.Glu510=
XM_011519021.1:c.1555G=	XP_011517323.1:p.Glu519=
XM_011519022.1:c.1552G=	XP_011517324.1:p.Glu518=
XM_011519023.1:c.1534G=	XP_011517325.1:p.Glu512=
XM_011519024.1:c.1477G=	XP_011517326.1:p.Glu493=
XM_011519025.1:c.1453G=	XP_011517327.1:p.Glu485=
XM_011519026.1:c.1555G=	XP_011517328.1:p.Glu519=
XM_011519027.1:c.1555G=	XP_011517329.1:p.Glu519=
XM_011519028.1:c.1555G=	XP_011517330.1:p.Glu519=
XM_011519029.1:c.-24G=	XP_011517331.1:n.-24G=
XM_011519033.1:c.1534G=	XP_011517335.1:p.Glu512=
NM_001354259.1:c.1453G=	NP_001341188.1:p.Glu485=
NM_001354263.1:c.1525G=	NP_001341192.1:p.Glu509=
NM_001354611.1:c.1546G=	NP_001341540.1:p.Glu516=
NM_001354612.1:c.1453G=	NP_001341541.1:p.Glu485=
XM_005266105.5:c.1537G=	XP_005266162.1:p.Glu513=
XM_011519021.3:c.1555G=	XP_011517323.1:p.Glu519=
XM_011519022.3:c.1552G=	XP_011517324.1:p.Glu518=
XM_011519023.3:c.1534G=	XP_011517325.1:p.Glu512=
XM_011519029.3:c.-24G=	XP_011517331.1:n.-24G=
XM_017015134.1:c.1531G=	XP_016870623.1:p.Glu511=
XM_017015136.2:c.1447G=	XP_016870625.1:p.Glu483=
XM_017015137.1:c.1432G=	XP_016870626.1:p.Glu478=
XM_017015138.1:c.1432G=	XP_016870627.1:p.Glu478=
XM_024447674.1:c.1375G=	XP_024303442.1:p.Glu459=
XM_024447675.1:c.1453G=	XP_024303443.1:p.Glu485=
XM_024447676.1:c.670G=	XP_024303444.1:p.Glu224=
XM_024447677.1:c.670G=	XP_024303445.1:p.Glu224=
XM_024447678.1:c.1453G=	XP_024303446.1:p.Glu485=
XM_024447679.1:c.1453G=	XP_024303447.1:p.Glu485=
XM_024447680.1:c.1432G=	XP_024303448.1:p.Glu478=
NM_024757.5:c.1546G= MANE Select	NP_079033.4:p.Glu516=
NM_001145527.2:c.1546G=	NP_001138999.1:p.Glu516=
NM_001354259.2:c.1453G=	NP_001341188.1:p.Glu485=
NM_001354263.2:c.1525G=	NP_001341192.1:p.Glu509=
NM_001354611.2:c.1546G=	NP_001341540.1:p.Glu516=
NM_001354612.2:c.1453G=	NP_001341541.1:p.Glu485=