Canonical Allele Identifier: CA287175984

Gene: ENO3

Linked Data

• ClinVar Variation Id: 2165186
• ClinVar RCV Id: RCV003084240
• dbSNP Id: rs903062624
• gnomAD v3: 17-4955292-A-G
• gnomAD v4: 17-4955292-A-G
• MyVariant Identifiers: chr17:g.4858587A>G (hg19) ; chr17:g.4955292A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955292A>G , CM000679.2:g.4955292A>G	GRCh38
NC_000017.10:g.4858587A>G , CM000679.1:g.4858587A>G	GRCh37
NC_000017.9:g.4799333A>G	NCBI36
NG_012063.2:g.14202A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.662A>G MANE Select	ENSP00000430055.2:p.Asn221Ser
ENST00000323997.10:c.662A>G	ENSP00000324105.6:p.Asn221Ser
ENST00000518175.1:c.662A>G	ENSP00000431087.1:p.Asn221Ser
ENST00000519584.5:c.533A>G	ENSP00000430636.1:p.Asn178Ser
ENST00000519602.5:c.662A>G	ENSP00000430055.1:p.Asn221Ser
ENST00000521659.5:c.*608A>G	ENSP00000430554.1:n.*608A>G
NM_001193503.1:c.533A>G	NP_001180432.1:p.Asn178Ser
NM_001976.4:c.662A>G	NP_001967.3:p.Asn221Ser
NM_053013.3:c.662A>G	NP_443739.3:p.Asn221Ser
XM_005256521.2:c.689A>G	XP_005256578.1:p.Asn230Ser
XM_011523729.1:c.662A>G	XP_011522031.1:p.Asn221Ser
XM_017024346.2:c.662A>G	XP_016879835.1:p.Asn221Ser
NM_001193503.2:c.533A>G	NP_001180432.1:p.Asn178Ser
NM_001374523.1:c.662A>G	NP_001361452.1:p.Asn221Ser
NM_001374524.1:c.689A>G	NP_001361453.1:p.Asn230Ser
NM_001976.5:c.662A>G	NP_001967.3:p.Asn221Ser
NM_053013.4:c.662A>G MANE Select	NP_443739.3:p.Asn221Ser