Canonical Allele Identifier: CA497679301
Gene: ENO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4858405A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4955110A>G , CM000679.2:g.4955110A>G GRCh38
NC_000017.10:g.4858405A>G , CM000679.1:g.4858405A>G GRCh37
NC_000017.9:g.4799151A>G NCBI36
NG_012063.2:g.14020A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000519602.6:c.480A>G MANE Select ENSP00000430055.2:p.Gly160=
ENST00000323997.10:c.480A>G ENSP00000324105.6:p.Gly160=
ENST00000518175.1:c.480A>G ENSP00000431087.1:p.Gly160=
ENST00000519584.5:c.351A>G ENSP00000430636.1:p.Gly117=
ENST00000519602.5:c.480A>G ENSP00000430055.1:p.Gly160=
ENST00000520221.5:c.480A>G ENSP00000467444.1:p.Gly160=
ENST00000521659.5:c.*426A>G ENSP00000430554.1:n.*426A>G
ENST00000522301.5:c.480A>G ENSP00000465697.1:p.Gly160=
NM_001193503.1:c.351A>G NP_001180432.1:p.Gly117=
NM_001976.4:c.480A>G NP_001967.3:p.Gly160=
NM_053013.3:c.480A>G NP_443739.3:p.Gly160=
XM_005256521.2:c.507A>G XP_005256578.1:p.Gly169=
XM_011523729.1:c.480A>G XP_011522031.1:p.Gly160=
XM_017024346.2:c.480A>G XP_016879835.1:p.Gly160=
NM_001193503.2:c.351A>G NP_001180432.1:p.Gly117=
NM_001374523.1:c.480A>G NP_001361452.1:p.Gly160=
NM_001374524.1:c.507A>G NP_001361453.1:p.Gly169=
NM_001976.5:c.480A>G NP_001967.3:p.Gly160=
NM_053013.4:c.480A>G MANE Select NP_443739.3:p.Gly160=