Canonical Allele Identifier: CA1884657146

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137757981G= , CM000671.2:g.137757981G=	GRCh38
NC_000009.11:g.140652433G= , CM000671.1:g.140652433G=	GRCh37
NC_000009.10:g.139772254G=	NCBI36
NG_011776.1:g.143990G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1471G= MANE Select	ENSP00000417980.1:p.Val491=
ENST00000629335.2:c.1471G=	ENSP00000490056.1:p.Val491=
ENST00000636027.1:c.1357G=	ENSP00000489961.1:p.Val453=
ENST00000637161.1:c.1378G=	ENSP00000490328.1:p.Val460=
ENST00000637261.1:c.1511G=	ENSP00000490815.1:n.1511G=
ENST00000637977.1:c.1416G=
ENST00000638071.1:c.1098G=
ENST00000640639.1:c.640G=	ENSP00000491823.1:p.Val214=
ENST00000371394.6:c.*1206G=	ENSP00000485945.1:n.*1206G=
ENST00000460843.5:c.1471G=	ENSP00000417980.1:p.Val491=
ENST00000462484.5:c.1471G=	ENSP00000417328.1:p.Val491=
ENST00000462942.3:c.328G=	ENSP00000436107.1:p.Val110=
ENST00000465566.2:c.163G=	ENSP00000486261.1:p.Val55=
ENST00000629808.2:c.564G=
NM_001145527.1:c.1471G=	NP_001138999.1:p.Val491=
NM_024757.4:c.1471G=	NP_079033.4:p.Val491=
XM_005266105.3:c.1462G=	XP_005266162.1:p.Val488=
XM_005266110.1:c.1378G=	XP_005266167.1:p.Val460=
XM_006717288.2:c.1453G=	XP_006717351.1:p.Val485=
XM_011519021.1:c.1480G=	XP_011517323.1:p.Val494=
XM_011519022.1:c.1477G=	XP_011517324.1:p.Val493=
XM_011519023.1:c.1459G=	XP_011517325.1:p.Val487=
XM_011519024.1:c.1402G=	XP_011517326.1:p.Val468=
XM_011519025.1:c.1378G=	XP_011517327.1:p.Val460=
XM_011519026.1:c.1480G=	XP_011517328.1:p.Val494=
XM_011519027.1:c.1480G=	XP_011517329.1:p.Val494=
XM_011519028.1:c.1480G=	XP_011517330.1:p.Val494=
XM_011519033.1:c.1459G=	XP_011517335.1:p.Val487=
NM_001354259.1:c.1378G=	NP_001341188.1:p.Val460=
NM_001354263.1:c.1450G=	NP_001341192.1:p.Val484=
NM_001354611.1:c.1471G=	NP_001341540.1:p.Val491=
NM_001354612.1:c.1378G=	NP_001341541.1:p.Val460=
XM_005266105.5:c.1462G=	XP_005266162.1:p.Val488=
XM_011519021.3:c.1480G=	XP_011517323.1:p.Val494=
XM_011519022.3:c.1477G=	XP_011517324.1:p.Val493=
XM_011519023.3:c.1459G=	XP_011517325.1:p.Val487=
XM_017015134.1:c.1456G=	XP_016870623.1:p.Val486=
XM_017015136.2:c.1372G=	XP_016870625.1:p.Val458=
XM_017015137.1:c.1357G=	XP_016870626.1:p.Val453=
XM_017015138.1:c.1357G=	XP_016870627.1:p.Val453=
XM_024447674.1:c.1300G=	XP_024303442.1:p.Val434=
XM_024447675.1:c.1378G=	XP_024303443.1:p.Val460=
XM_024447676.1:c.595G=	XP_024303444.1:p.Val199=
XM_024447677.1:c.595G=	XP_024303445.1:p.Val199=
XM_024447678.1:c.1378G=	XP_024303446.1:p.Val460=
XM_024447679.1:c.1378G=	XP_024303447.1:p.Val460=
XM_024447680.1:c.1357G=	XP_024303448.1:p.Val453=
NM_024757.5:c.1471G= MANE Select	NP_079033.4:p.Val491=
NM_001145527.2:c.1471G=	NP_001138999.1:p.Val491=
NM_001354259.2:c.1378G=	NP_001341188.1:p.Val460=
NM_001354263.2:c.1450G=	NP_001341192.1:p.Val484=
NM_001354611.2:c.1471G=	NP_001341540.1:p.Val491=
NM_001354612.2:c.1378G=	NP_001341541.1:p.Val460=