Canonical Allele Identifier: CA2691006982
Gene: ALDOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425138_101425139insACA , CM000671.2:g.101425138_101425139insACA GRCh38
NC_000009.11:g.104187420_104187421insACA , CM000671.1:g.104187420_104187421insACA GRCh37
NC_000009.10:g.103227241_103227242insACA NCBI36
NG_012387.1:g.15642_15643insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.800-97_800-96insTGT MANE Select ENSP00000497767.1:n.800-97_800-96insTGT
ENST00000648064.1:c.800-97_800-96insTGT ENSP00000497990.1:n.800-97_800-96insTGT
ENST00000648758.1:c.800-97_800-96insTGT ENSP00000497731.1:n.800-97_800-96insTGT
ENST00000649902.1:c.800-97_800-96insTGT ENSP00000497216.1:n.800-97_800-96insTGT
ENST00000374855.8:c.800-97_800-96insTGT ENSP00000363988.4:n.800-97_800-96insTGT
ENST00000616752.1:c.800-97_800-96insTGT ENSP00000481363.1:n.800-97_800-96insTGT
NM_000035.3:c.800-97_800-96insTGT NP_000026.2:n.800-97_800-96insTGT
NM_000035.4:c.800-97_800-96insTGT MANE Select NP_000026.2:n.800-97_800-96insTGT