Canonical Allele Identifier: CA1884666523

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776812C= , CM000671.2:g.137776812C=	GRCh38
NC_000009.11:g.140671264C= , CM000671.1:g.140671264C=	GRCh37
NC_000009.10:g.139791085C=	NCBI36
NG_011776.1:g.162821C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1986C= MANE Select	ENSP00000417980.1:p.Ala662=
ENST00000636027.1:c.1872C=	ENSP00000489961.1:p.Ala624=
ENST00000637161.1:c.1893C=	ENSP00000490328.1:p.Ala631=
ENST00000637261.1:c.2026C=	ENSP00000490815.1:n.2026C=
ENST00000638071.1:c.1613C=
ENST00000640639.1:c.1155C=	ENSP00000491823.1:p.Ala385=
ENST00000371394.6:c.*1721C=	ENSP00000485945.1:n.*1721C=
ENST00000460843.5:c.1986C=	ENSP00000417980.1:p.Ala662=
ENST00000462484.5:c.1986C=	ENSP00000417328.1:p.Ala662=
ENST00000462942.3:c.843C=	ENSP00000436107.1:p.Ala281=
ENST00000626603.1:n.1637G=
NM_001145527.1:c.1986C=	NP_001138999.1:p.Ala662=
NM_024757.4:c.1986C=	NP_079033.4:p.Ala662=
XM_005266105.3:c.1977C=	XP_005266162.1:p.Ala659=
XM_005266110.1:c.1893C=	XP_005266167.1:p.Ala631=
XM_006717288.2:c.1968C=	XP_006717351.1:p.Ala656=
XM_011519021.1:c.1995C=	XP_011517323.1:p.Ala665=
XM_011519022.1:c.1992C=	XP_011517324.1:p.Ala664=
XM_011519023.1:c.1974C=	XP_011517325.1:p.Ala658=
XM_011519024.1:c.1917C=	XP_011517326.1:p.Ala639=
XM_011519025.1:c.1893C=	XP_011517327.1:p.Ala631=
XM_011519026.1:c.1851C=	XP_011517328.1:p.Ala617=
XM_011519027.1:c.1995C=	XP_011517329.1:p.Ala665=
XM_011519028.1:c.1995C=	XP_011517330.1:p.Ala665=
XM_011519029.1:c.417C=	XP_011517331.1:p.Ala139=
XM_011519033.1:c.1830C=	XP_011517335.1:p.Ala610=
NM_001354259.1:c.1893C=	NP_001341188.1:p.Ala631=
NM_001354263.1:c.1965C=	NP_001341192.1:p.Ala655=
XM_005266105.5:c.1977C=	XP_005266162.1:p.Ala659=
XM_011519021.3:c.1995C=	XP_011517323.1:p.Ala665=
XM_011519022.3:c.1992C=	XP_011517324.1:p.Ala664=
XM_011519023.3:c.1974C=	XP_011517325.1:p.Ala658=
XM_011519029.3:c.417C=	XP_011517331.1:p.Ala139=
XM_017015134.1:c.1971C=	XP_016870623.1:p.Ala657=
XM_017015136.2:c.1887C=	XP_016870625.1:p.Ala629=
XM_017015137.1:c.1872C=	XP_016870626.1:p.Ala624=
XM_017015138.1:c.1872C=	XP_016870627.1:p.Ala624=
XM_024447674.1:c.1815C=	XP_024303442.1:p.Ala605=
XM_024447675.1:c.1749C=	XP_024303443.1:p.Ala583=
XM_024447676.1:c.1110C=	XP_024303444.1:p.Ala370=
XM_024447677.1:c.1110C=	XP_024303445.1:p.Ala370=
XM_024447678.1:c.1893C=	XP_024303446.1:p.Ala631=
XM_024447679.1:c.1893C=	XP_024303447.1:p.Ala631=
XM_024447680.1:c.1728C=	XP_024303448.1:p.Ala576=
NM_024757.5:c.1986C= MANE Select	NP_079033.4:p.Ala662=
NM_001145527.2:c.1986C=	NP_001138999.1:p.Ala662=
NM_001354259.2:c.1893C=	NP_001341188.1:p.Ala631=
NM_001354263.2:c.1965C=	NP_001341192.1:p.Ala655=