Canonical Allele Identifier: CA624856850

Gene: ENO3

Linked Data

• dbSNP Id: rs1380153867
• gnomAD v2: 17-4858668-T-TG
• gnomAD v4: 17-4955373-T-TG
• MyVariant Identifiers: chr17:g.4858668_4858669insG (hg19) ; chr17:g.4955373_4955374insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955375dup , CM000679.2:g.4955375dup	GRCh38
NC_000017.10:g.4858670dup , CM000679.1:g.4858670dup	GRCh37
NC_000017.9:g.4799416dup	NCBI36
NG_012063.2:g.14285dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.668-32dup MANE Select	ENSP00000430055.2:n.668-32dup
ENST00000323997.10:c.668-32dup	ENSP00000324105.6:n.668-32dup
ENST00000518175.1:c.668-32dup	ENSP00000431087.1:n.668-32dup
ENST00000519584.5:c.539-32dup	ENSP00000430636.1:n.539-32dup
ENST00000519602.5:c.668-32dup	ENSP00000430055.1:n.668-32dup
ENST00000521659.5:c.*614-32dup	ENSP00000430554.1:n.*614-32dup
NM_001193503.1:c.539-32dup	NP_001180432.1:n.539-32dup
NM_001976.4:c.668-32dup	NP_001967.3:n.668-32dup
NM_053013.3:c.668-32dup	NP_443739.3:n.668-32dup
XM_005256521.2:c.695-32dup	XP_005256578.1:n.695-32dup
XM_011523729.1:c.668-32dup	XP_011522031.1:n.668-32dup
XM_017024346.2:c.668-32dup	XP_016879835.1:n.668-32dup
NM_001193503.2:c.539-32dup	NP_001180432.1:n.539-32dup
NM_001374523.1:c.668-32dup	NP_001361452.1:n.668-32dup
NM_001374524.1:c.695-32dup	NP_001361453.1:n.695-32dup
NM_001976.5:c.668-32dup	NP_001967.3:n.668-32dup
NM_053013.4:c.668-32dup MANE Select	NP_443739.3:n.668-32dup