Canonical Allele Identifier: CA2244628375

Gene: ENO3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955226A= , CM000679.2:g.4955226A=	GRCh38
NC_000017.10:g.4858521A= , CM000679.1:g.4858521A=	GRCh37
NC_000017.9:g.4799267A=	NCBI36
NG_012063.2:g.14136A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.596A= MANE Select	ENSP00000430055.2:p.Lys199=
ENST00000323997.10:c.596A=	ENSP00000324105.6:p.Lys199=
ENST00000518175.1:c.596A=	ENSP00000431087.1:p.Lys199=
ENST00000519584.5:c.467A=	ENSP00000430636.1:p.Lys156=
ENST00000519602.5:c.596A=	ENSP00000430055.1:p.Lys199=
ENST00000521659.5:c.*542A=	ENSP00000430554.1:n.*542A=
ENST00000522301.5:c.596A=	ENSP00000465697.1:p.Lys199=
NM_001193503.1:c.467A=	NP_001180432.1:p.Lys156=
NM_001976.4:c.596A=	NP_001967.3:p.Lys199=
NM_053013.3:c.596A=	NP_443739.3:p.Lys199=
XM_005256521.2:c.623A=	XP_005256578.1:p.Lys208=
XM_011523729.1:c.596A=	XP_011522031.1:p.Lys199=
XM_017024346.2:c.596A=	XP_016879835.1:p.Lys199=
NM_001193503.2:c.467A=	NP_001180432.1:p.Lys156=
NM_001374523.1:c.596A=	NP_001361452.1:p.Lys199=
NM_001374524.1:c.623A=	NP_001361453.1:p.Lys208=
NM_001976.5:c.596A=	NP_001967.3:p.Lys199=
NM_053013.4:c.596A= MANE Select	NP_443739.3:p.Lys199=