Canonical Allele Identifier: CA1884666526

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776820G= , CM000671.2:g.137776820G=	GRCh38
NC_000009.11:g.140671272G= , CM000671.1:g.140671272G=	GRCh37
NC_000009.10:g.139791093G=	NCBI36
NG_011776.1:g.162829G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1994G= MANE Select	ENSP00000417980.1:p.Gly665=
ENST00000636027.1:c.1880G=	ENSP00000489961.1:p.Gly627=
ENST00000637161.1:c.1901G=	ENSP00000490328.1:p.Gly634=
ENST00000637261.1:c.2034G=	ENSP00000490815.1:n.2034G=
ENST00000638071.1:c.1621G=
ENST00000640639.1:c.1163G=	ENSP00000491823.1:p.Gly388=
ENST00000371394.6:c.*1729G=	ENSP00000485945.1:n.*1729G=
ENST00000460843.5:c.1994G=	ENSP00000417980.1:p.Gly665=
ENST00000462484.5:c.1994G=	ENSP00000417328.1:p.Gly665=
ENST00000462942.3:c.851G=	ENSP00000436107.1:p.Gly284=
ENST00000626603.1:n.1629C=
NM_001145527.1:c.1994G=	NP_001138999.1:p.Gly665=
NM_024757.4:c.1994G=	NP_079033.4:p.Gly665=
XM_005266105.3:c.1985G=	XP_005266162.1:p.Gly662=
XM_005266110.1:c.1901G=	XP_005266167.1:p.Gly634=
XM_006717288.2:c.1976G=	XP_006717351.1:p.Gly659=
XM_011519021.1:c.2003G=	XP_011517323.1:p.Gly668=
XM_011519022.1:c.2000G=	XP_011517324.1:p.Gly667=
XM_011519023.1:c.1982G=	XP_011517325.1:p.Gly661=
XM_011519024.1:c.1925G=	XP_011517326.1:p.Gly642=
XM_011519025.1:c.1901G=	XP_011517327.1:p.Gly634=
XM_011519026.1:c.1859G=	XP_011517328.1:p.Gly620=
XM_011519027.1:c.2003G=	XP_011517329.1:p.Gly668=
XM_011519028.1:c.2003G=	XP_011517330.1:p.Gly668=
XM_011519029.1:c.425G=	XP_011517331.1:p.Gly142=
XM_011519033.1:c.1838G=	XP_011517335.1:p.Gly613=
NM_001354259.1:c.1901G=	NP_001341188.1:p.Gly634=
NM_001354263.1:c.1973G=	NP_001341192.1:p.Gly658=
XM_005266105.5:c.1985G=	XP_005266162.1:p.Gly662=
XM_011519021.3:c.2003G=	XP_011517323.1:p.Gly668=
XM_011519022.3:c.2000G=	XP_011517324.1:p.Gly667=
XM_011519023.3:c.1982G=	XP_011517325.1:p.Gly661=
XM_011519029.3:c.425G=	XP_011517331.1:p.Gly142=
XM_017015134.1:c.1979G=	XP_016870623.1:p.Gly660=
XM_017015136.2:c.1895G=	XP_016870625.1:p.Gly632=
XM_017015137.1:c.1880G=	XP_016870626.1:p.Gly627=
XM_017015138.1:c.1880G=	XP_016870627.1:p.Gly627=
XM_024447674.1:c.1823G=	XP_024303442.1:p.Gly608=
XM_024447675.1:c.1757G=	XP_024303443.1:p.Gly586=
XM_024447676.1:c.1118G=	XP_024303444.1:p.Gly373=
XM_024447677.1:c.1118G=	XP_024303445.1:p.Gly373=
XM_024447678.1:c.1901G=	XP_024303446.1:p.Gly634=
XM_024447679.1:c.1901G=	XP_024303447.1:p.Gly634=
XM_024447680.1:c.1736G=	XP_024303448.1:p.Gly579=
NM_024757.5:c.1994G= MANE Select	NP_079033.4:p.Gly665=
NM_001145527.2:c.1994G=	NP_001138999.1:p.Gly665=
NM_001354259.2:c.1901G=	NP_001341188.1:p.Gly634=
NM_001354263.2:c.1973G=	NP_001341192.1:p.Gly658=