Canonical Allele Identifier: CA1868275380
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421658_101421659delinsAT , CM000671.2:g.101421658_101421659delinsAT GRCh38
NC_000009.11:g.104183940_104183941delinsAT , CM000671.1:g.104183940_104183941delinsAT GRCh37
NC_000009.10:g.103223761_103223762delinsAT NCBI36
NG_012387.1:g.19122_19123delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.*150_*151delinsAT MANE Select ENSP00000497767.1:n.*150_*151delinsAT
ENST00000648064.1:c.*150_*151delinsAT ENSP00000497990.1:n.*150_*151delinsAT
ENST00000648758.1:c.*150_*151delinsAT ENSP00000497731.1:n.*150_*151delinsAT
ENST00000374855.8:c.*150_*151delinsAT ENSP00000363988.4:n.*150_*151delinsAT
ENST00000616752.1:c.*257_*258delinsAT ENSP00000481363.1:n.*257_*258delinsAT
NM_000035.3:c.*150_*151delinsAT NP_000026.2:n.*150_*151delinsAT
NM_000035.4:c.*150_*151delinsAT MANE Select NP_000026.2:n.*150_*151delinsAT