Canonical Allele Identifier: CA497679483

Gene: ENO3

Linked Data

• ClinVar Variation Id: 1959986
• ClinVar RCV Id: RCV002701555 ; RCV003926433
• MyVariant Identifiers: chr17:g.4858709G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955414G>A , CM000679.2:g.4955414G>A	GRCh38
NC_000017.10:g.4858709G>A , CM000679.1:g.4858709G>A	GRCh37
NC_000017.9:g.4799455G>A	NCBI36
NG_012063.2:g.14324G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.675G>A MANE Select	ENSP00000430055.2:p.Glu225=
ENST00000323997.10:c.675G>A	ENSP00000324105.6:p.Glu225=
ENST00000518175.1:c.675G>A	ENSP00000431087.1:p.Glu225=
ENST00000519584.5:c.546G>A	ENSP00000430636.1:p.Glu182=
ENST00000519602.5:c.675G>A	ENSP00000430055.1:p.Glu225=
ENST00000521659.5:c.*621G>A	ENSP00000430554.1:n.*621G>A
NM_001193503.1:c.546G>A	NP_001180432.1:p.Glu182=
NM_001976.4:c.675G>A	NP_001967.3:p.Glu225=
NM_053013.3:c.675G>A	NP_443739.3:p.Glu225=
XM_005256521.2:c.702G>A	XP_005256578.1:p.Glu234=
XM_011523729.1:c.675G>A	XP_011522031.1:p.Glu225=
XM_017024346.2:c.675G>A	XP_016879835.1:p.Glu225=
NM_001193503.2:c.546G>A	NP_001180432.1:p.Glu182=
NM_001374523.1:c.675G>A	NP_001361452.1:p.Glu225=
NM_001374524.1:c.702G>A	NP_001361453.1:p.Glu234=
NM_001976.5:c.675G>A	NP_001967.3:p.Glu225=
NM_053013.4:c.675G>A MANE Select	NP_443739.3:p.Glu225=