Canonical Allele Identifier: CA2244628179

Gene: ENO3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955140T= , CM000679.2:g.4955140T=	GRCh38
NC_000017.10:g.4858435T= , CM000679.1:g.4858435T=	GRCh37
NC_000017.9:g.4799181T=	NCBI36
NG_012063.2:g.14050T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.510T= MANE Select	ENSP00000430055.2:p.Ile170=
ENST00000323997.10:c.510T=	ENSP00000324105.6:p.Ile170=
ENST00000518175.1:c.510T=	ENSP00000431087.1:p.Ile170=
ENST00000519584.5:c.381T=	ENSP00000430636.1:p.Ile127=
ENST00000519602.5:c.510T=	ENSP00000430055.1:p.Ile170=
ENST00000520221.5:c.510T=	ENSP00000467444.1:p.Ile170=
ENST00000521659.5:c.*456T=	ENSP00000430554.1:n.*456T=
ENST00000522301.5:c.510T=	ENSP00000465697.1:p.Ile170=
NM_001193503.1:c.381T=	NP_001180432.1:p.Ile127=
NM_001976.4:c.510T=	NP_001967.3:p.Ile170=
NM_053013.3:c.510T=	NP_443739.3:p.Ile170=
XM_005256521.2:c.537T=	XP_005256578.1:p.Ile179=
XM_011523729.1:c.510T=	XP_011522031.1:p.Ile170=
XM_017024346.2:c.510T=	XP_016879835.1:p.Ile170=
NM_001193503.2:c.381T=	NP_001180432.1:p.Ile127=
NM_001374523.1:c.510T=	NP_001361452.1:p.Ile170=
NM_001374524.1:c.537T=	NP_001361453.1:p.Ile179=
NM_001976.5:c.510T=	NP_001967.3:p.Ile170=
NM_053013.4:c.510T= MANE Select	NP_443739.3:p.Ile170=