Canonical Allele Identifier: CA374264636
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425467G>A , CM000671.2:g.101425467G>A GRCh38
NC_000009.11:g.104187749G>A , CM000671.1:g.104187749G>A GRCh37
NC_000009.10:g.103227570G>A NCBI36
NG_012387.1:g.15314C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.785C>T MANE Select ENSP00000497767.1:p.Pro262Leu
ENST00000648064.1:c.785C>T ENSP00000497990.1:p.Pro262Leu
ENST00000648758.1:c.785C>T ENSP00000497731.1:p.Pro262Leu
ENST00000649902.1:c.785C>T ENSP00000497216.1:p.Pro262Leu
ENST00000374855.8:c.785C>T ENSP00000363988.4:p.Pro262Leu
ENST00000616752.1:c.785C>T ENSP00000481363.1:p.Pro262Leu
NM_000035.3:c.785C>T NP_000026.2:p.Pro262Leu
NM_000035.4:c.785C>T MANE Select NP_000026.2:p.Pro262Leu