Canonical Allele Identifier: CA1868281045
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101429659_101429662delinsTGAG , CM000671.2:g.101429659_101429662delinsTGAG GRCh38
NC_000009.11:g.104191941_104191944delinsTGAG , CM000671.1:g.104191941_104191944delinsTGAG GRCh37
NC_000009.10:g.103231762_103231765delinsTGAG NCBI36
NG_012387.1:g.11119_11122delinsCTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.324+93_324+96delinsCTCA MANE Select ENSP00000497767.1:n.324+93_324+96delinsCT...
ENST00000648064.1:c.324+93_324+96delinsCTCA ENSP00000497990.1:n.324+93_324+96delinsCT...
ENST00000648758.1:c.324+93_324+96delinsCTCA ENSP00000497731.1:n.324+93_324+96delinsCT...
ENST00000648906.1:n.587_590delinsCTCA
ENST00000649902.1:c.324+93_324+96delinsCTCA ENSP00000497216.1:n.324+93_324+96delinsCT...
ENST00000650613.1:n.493_496delinsCTCA
ENST00000374855.8:c.324+93_324+96delinsCTCA ENSP00000363988.4:n.324+93_324+96delinsCT...
ENST00000468981.3:n.67+147_67+150delinsCTCA
ENST00000616752.1:c.324+93_324+96delinsCTCA ENSP00000481363.1:n.324+93_324+96delinsCT...
NM_000035.3:c.324+93_324+96delinsCTCA NP_000026.2:n.324+93_324+96delinsCTCA
NM_000035.4:c.324+93_324+96delinsCTCA MANE Select NP_000026.2:n.324+93_324+96delinsCTCA
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