Canonical Allele Identifier: CA2695199394
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2675446
ClinVar RCV Id: RCV003460165

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425601_101426915delinsAACCCAT , CM000671.2:g.101425601_101426915delinsAACCCAT GRCh38
NC_000009.11:g.104187883_104189197delinsAACCCAT , CM000671.1:g.104187883_104189197delinsAACCCAT GRCh37
NC_000009.10:g.103227704_103229018delinsAACCCAT NCBI36
NG_012387.1:g.13866_15180delinsATGGGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.541-277_651delinsATGGGTT
ENST00000648064.1:c.541-277_651delinsATGGGTT
ENST00000648758.1:c.541-277_651delinsATGGGTT
ENST00000649902.1:c.541-277_651delinsATGGGTT
ENST00000374855.8:c.541-277_651delinsATGGGTT
ENST00000468981.3:n.68-277_178delinsATGGGTT
ENST00000616752.1:c.541-277_651delinsATGGGTT
NM_000035.3:c.541-277_651delinsATGGGTT
NM_000035.4:c.541-277_651delinsATGGGTT