Canonical Allele Identifier: CA1884666520

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776808C= , CM000671.2:g.137776808C=	GRCh38
NC_000009.11:g.140671260C= , CM000671.1:g.140671260C=	GRCh37
NC_000009.10:g.139791081C=	NCBI36
NG_011776.1:g.162817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1982C= MANE Select	ENSP00000417980.1:p.Ser661=
ENST00000636027.1:c.1868C=	ENSP00000489961.1:p.Ser623=
ENST00000637161.1:c.1889C=	ENSP00000490328.1:p.Ser630=
ENST00000637261.1:c.2022C=	ENSP00000490815.1:n.2022C=
ENST00000638071.1:c.1609C=
ENST00000640639.1:c.1151C=	ENSP00000491823.1:p.Ser384=
ENST00000371394.6:c.*1717C=	ENSP00000485945.1:n.*1717C=
ENST00000460843.5:c.1982C=	ENSP00000417980.1:p.Ser661=
ENST00000462484.5:c.1982C=	ENSP00000417328.1:p.Ser661=
ENST00000462942.3:c.839C=	ENSP00000436107.1:p.Ser280=
ENST00000626603.1:n.1641G=
NM_001145527.1:c.1982C=	NP_001138999.1:p.Ser661=
NM_024757.4:c.1982C=	NP_079033.4:p.Ser661=
XM_005266105.3:c.1973C=	XP_005266162.1:p.Ser658=
XM_005266110.1:c.1889C=	XP_005266167.1:p.Ser630=
XM_006717288.2:c.1964C=	XP_006717351.1:p.Ser655=
XM_011519021.1:c.1991C=	XP_011517323.1:p.Ser664=
XM_011519022.1:c.1988C=	XP_011517324.1:p.Ser663=
XM_011519023.1:c.1970C=	XP_011517325.1:p.Ser657=
XM_011519024.1:c.1913C=	XP_011517326.1:p.Ser638=
XM_011519025.1:c.1889C=	XP_011517327.1:p.Ser630=
XM_011519026.1:c.1847C=	XP_011517328.1:p.Ser616=
XM_011519027.1:c.1991C=	XP_011517329.1:p.Ser664=
XM_011519028.1:c.1991C=	XP_011517330.1:p.Ser664=
XM_011519029.1:c.413C=	XP_011517331.1:p.Ser138=
XM_011519033.1:c.1826C=	XP_011517335.1:p.Ser609=
NM_001354259.1:c.1889C=	NP_001341188.1:p.Ser630=
NM_001354263.1:c.1961C=	NP_001341192.1:p.Ser654=
XM_005266105.5:c.1973C=	XP_005266162.1:p.Ser658=
XM_011519021.3:c.1991C=	XP_011517323.1:p.Ser664=
XM_011519022.3:c.1988C=	XP_011517324.1:p.Ser663=
XM_011519023.3:c.1970C=	XP_011517325.1:p.Ser657=
XM_011519029.3:c.413C=	XP_011517331.1:p.Ser138=
XM_017015134.1:c.1967C=	XP_016870623.1:p.Ser656=
XM_017015136.2:c.1883C=	XP_016870625.1:p.Ser628=
XM_017015137.1:c.1868C=	XP_016870626.1:p.Ser623=
XM_017015138.1:c.1868C=	XP_016870627.1:p.Ser623=
XM_024447674.1:c.1811C=	XP_024303442.1:p.Ser604=
XM_024447675.1:c.1745C=	XP_024303443.1:p.Ser582=
XM_024447676.1:c.1106C=	XP_024303444.1:p.Ser369=
XM_024447677.1:c.1106C=	XP_024303445.1:p.Ser369=
XM_024447678.1:c.1889C=	XP_024303446.1:p.Ser630=
XM_024447679.1:c.1889C=	XP_024303447.1:p.Ser630=
XM_024447680.1:c.1724C=	XP_024303448.1:p.Ser575=
NM_024757.5:c.1982C= MANE Select	NP_079033.4:p.Ser661=
NM_001145527.2:c.1982C=	NP_001138999.1:p.Ser661=
NM_001354259.2:c.1889C=	NP_001341188.1:p.Ser630=
NM_001354263.2:c.1961C=	NP_001341192.1:p.Ser654=