Canonical Allele Identifier: CA397289800
Gene: ENO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4955103A>T , CM000679.2:g.4955103A>T GRCh38
NC_000017.10:g.4858398A>T , CM000679.1:g.4858398A>T GRCh37
NC_000017.9:g.4799144A>T NCBI36
NG_012063.2:g.14013A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000519602.6:c.473A>T MANE Select ENSP00000430055.2:p.His158Leu
ENST00000323997.10:c.473A>T ENSP00000324105.6:p.His158Leu
ENST00000518175.1:c.473A>T ENSP00000431087.1:p.His158Leu
ENST00000519584.5:c.344A>T ENSP00000430636.1:p.His115Leu
ENST00000519602.5:c.473A>T ENSP00000430055.1:p.His158Leu
ENST00000520221.5:c.473A>T ENSP00000467444.1:p.His158Leu
ENST00000521659.5:c.*419A>T ENSP00000430554.1:n.*419A>T
ENST00000522301.5:c.473A>T ENSP00000465697.1:p.His158Leu
NM_001193503.1:c.344A>T NP_001180432.1:p.His115Leu
NM_001976.4:c.473A>T NP_001967.3:p.His158Leu
NM_053013.3:c.473A>T NP_443739.3:p.His158Leu
XM_005256521.2:c.500A>T XP_005256578.1:p.His167Leu
XM_011523729.1:c.473A>T XP_011522031.1:p.His158Leu
XM_017024346.2:c.473A>T XP_016879835.1:p.His158Leu
NM_001193503.2:c.344A>T NP_001180432.1:p.His115Leu
NM_001374523.1:c.473A>T NP_001361452.1:p.His158Leu
NM_001374524.1:c.500A>T NP_001361453.1:p.His167Leu
NM_001976.5:c.473A>T NP_001967.3:p.His158Leu
NM_053013.4:c.473A>T MANE Select NP_443739.3:p.His158Leu