Canonical Allele Identifier: CA497679299
Gene: ENO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.4858402T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4955107T>G , CM000679.2:g.4955107T>G GRCh38
NC_000017.10:g.4858402T>G , CM000679.1:g.4858402T>G GRCh37
NC_000017.9:g.4799148T>G NCBI36
NG_012063.2:g.14017T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000519602.6:c.477T>G MANE Select ENSP00000430055.2:p.Ala159=
ENST00000323997.10:c.477T>G ENSP00000324105.6:p.Ala159=
ENST00000518175.1:c.477T>G ENSP00000431087.1:p.Ala159=
ENST00000519584.5:c.348T>G ENSP00000430636.1:p.Ala116=
ENST00000519602.5:c.477T>G ENSP00000430055.1:p.Ala159=
ENST00000520221.5:c.477T>G ENSP00000467444.1:p.Ala159=
ENST00000521659.5:c.*423T>G ENSP00000430554.1:n.*423T>G
ENST00000522301.5:c.477T>G ENSP00000465697.1:p.Ala159=
NM_001193503.1:c.348T>G NP_001180432.1:p.Ala116=
NM_001976.4:c.477T>G NP_001967.3:p.Ala159=
NM_053013.3:c.477T>G NP_443739.3:p.Ala159=
XM_005256521.2:c.504T>G XP_005256578.1:p.Ala168=
XM_011523729.1:c.477T>G XP_011522031.1:p.Ala159=
XM_017024346.2:c.477T>G XP_016879835.1:p.Ala159=
NM_001193503.2:c.348T>G NP_001180432.1:p.Ala116=
NM_001374523.1:c.477T>G NP_001361452.1:p.Ala159=
NM_001374524.1:c.504T>G NP_001361453.1:p.Ala168=
NM_001976.5:c.477T>G NP_001967.3:p.Ala159=
NM_053013.4:c.477T>G MANE Select NP_443739.3:p.Ala159=