Canonical Allele Identifier: CA397290528

Gene: ENO3

Linked Data

• MyVariant Identifiers: chr17:g.4858562T>G (hg19) ; chr17:g.4955267T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955267T>G , CM000679.2:g.4955267T>G	GRCh38
NC_000017.10:g.4858562T>G , CM000679.1:g.4858562T>G	GRCh37
NC_000017.9:g.4799308T>G	NCBI36
NG_012063.2:g.14177T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.637T>G MANE Select	ENSP00000430055.2:p.Phe213Val
ENST00000323997.10:c.637T>G	ENSP00000324105.6:p.Phe213Val
ENST00000518175.1:c.637T>G	ENSP00000431087.1:p.Phe213Val
ENST00000519584.5:c.508T>G	ENSP00000430636.1:p.Phe170Val
ENST00000519602.5:c.637T>G	ENSP00000430055.1:p.Phe213Val
ENST00000521659.5:c.*583T>G	ENSP00000430554.1:n.*583T>G
ENST00000522301.5:c.637T>G
NM_001193503.1:c.508T>G	NP_001180432.1:p.Phe170Val
NM_001976.4:c.637T>G	NP_001967.3:p.Phe213Val
NM_053013.3:c.637T>G	NP_443739.3:p.Phe213Val
XM_005256521.2:c.664T>G	XP_005256578.1:p.Phe222Val
XM_011523729.1:c.637T>G	XP_011522031.1:p.Phe213Val
XM_017024346.2:c.637T>G	XP_016879835.1:p.Phe213Val
NM_001193503.2:c.508T>G	NP_001180432.1:p.Phe170Val
NM_001374523.1:c.637T>G	NP_001361452.1:p.Phe213Val
NM_001374524.1:c.664T>G	NP_001361453.1:p.Phe222Val
NM_001976.5:c.637T>G	NP_001967.3:p.Phe213Val
NM_053013.4:c.637T>G MANE Select	NP_443739.3:p.Phe213Val