Canonical Allele Identifier: CA374265917
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429891A>G , CM000671.2:g.101429891A>G GRCh38
NC_000009.11:g.104192173A>G , CM000671.1:g.104192173A>G GRCh37
NC_000009.10:g.103231994A>G NCBI36
NG_012387.1:g.10890T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.188T>C MANE Select ENSP00000497767.1:p.Leu63Pro
ENST00000648064.1:c.188T>C ENSP00000497990.1:p.Leu63Pro
ENST00000648423.1:c.188T>C ENSP00000497985.1:p.Leu63Pro
ENST00000648758.1:c.188T>C ENSP00000497731.1:p.Leu63Pro
ENST00000648906.1:n.358T>C
ENST00000649902.1:c.188T>C ENSP00000497216.1:p.Leu63Pro
ENST00000650613.1:n.264T>C
ENST00000374855.8:c.188T>C ENSP00000363988.4:p.Leu63Pro
ENST00000616752.1:c.188T>C ENSP00000481363.1:p.Leu63Pro
NM_000035.3:c.188T>C NP_000026.2:p.Leu63Pro
NM_000035.4:c.188T>C MANE Select NP_000026.2:p.Leu63Pro