Canonical Allele Identifier: CA497679513

Gene: ENO3

Linked Data

• MyVariant Identifiers: chr17:g.4858736T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955441T>G , CM000679.2:g.4955441T>G	GRCh38
NC_000017.10:g.4858736T>G , CM000679.1:g.4858736T>G	GRCh37
NC_000017.9:g.4799482T>G	NCBI36
NG_012063.2:g.14351T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.702T>G MANE Select	ENSP00000430055.2:p.Ala234=
ENST00000323997.10:c.702T>G	ENSP00000324105.6:p.Ala234=
ENST00000518175.1:c.702T>G	ENSP00000431087.1:p.Ala234=
ENST00000519584.5:c.573T>G	ENSP00000430636.1:p.Ala191=
ENST00000519602.5:c.702T>G	ENSP00000430055.1:p.Ala234=
ENST00000521659.5:c.*648T>G	ENSP00000430554.1:n.*648T>G
NM_001193503.1:c.573T>G	NP_001180432.1:p.Ala191=
NM_001976.4:c.702T>G	NP_001967.3:p.Ala234=
NM_053013.3:c.702T>G	NP_443739.3:p.Ala234=
XM_005256521.2:c.729T>G	XP_005256578.1:p.Ala243=
XM_011523729.1:c.702T>G	XP_011522031.1:p.Ala234=
XM_017024346.2:c.702T>G	XP_016879835.1:p.Ala234=
NM_001193503.2:c.573T>G	NP_001180432.1:p.Ala191=
NM_001374523.1:c.702T>G	NP_001361452.1:p.Ala234=
NM_001374524.1:c.729T>G	NP_001361453.1:p.Ala243=
NM_001976.5:c.702T>G	NP_001967.3:p.Ala234=
NM_053013.4:c.702T>G MANE Select	NP_443739.3:p.Ala234=