Canonical Allele Identifier: CA2244628244

Gene: ENO3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955172C= , CM000679.2:g.4955172C=	GRCh38
NC_000017.10:g.4858467C= , CM000679.1:g.4858467C=	GRCh37
NC_000017.9:g.4799213C=	NCBI36
NG_012063.2:g.14082C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.542C= MANE Select	ENSP00000430055.2:p.Ala181=
ENST00000323997.10:c.542C=	ENSP00000324105.6:p.Ala181=
ENST00000518175.1:c.542C=	ENSP00000431087.1:p.Ala181=
ENST00000519584.5:c.413C=	ENSP00000430636.1:p.Ala138=
ENST00000519602.5:c.542C=	ENSP00000430055.1:p.Ala181=
ENST00000520221.5:c.542C=	ENSP00000467444.1:p.Ala181=
ENST00000521659.5:c.*488C=	ENSP00000430554.1:n.*488C=
ENST00000522301.5:c.542C=	ENSP00000465697.1:p.Ala181=
NM_001193503.1:c.413C=	NP_001180432.1:p.Ala138=
NM_001976.4:c.542C=	NP_001967.3:p.Ala181=
NM_053013.3:c.542C=	NP_443739.3:p.Ala181=
XM_005256521.2:c.569C=	XP_005256578.1:p.Ala190=
XM_011523729.1:c.542C=	XP_011522031.1:p.Ala181=
XM_017024346.2:c.542C=	XP_016879835.1:p.Ala181=
NM_001193503.2:c.413C=	NP_001180432.1:p.Ala138=
NM_001374523.1:c.542C=	NP_001361452.1:p.Ala181=
NM_001374524.1:c.569C=	NP_001361453.1:p.Ala190=
NM_001976.5:c.542C=	NP_001967.3:p.Ala181=
NM_053013.4:c.542C= MANE Select	NP_443739.3:p.Ala181=