Canonical Allele Identifier: CA1868275534
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101421786_101421788delinsGCT , CM000671.2:g.101421786_101421788delinsGCT GRCh38
NC_000009.11:g.104184068_104184070delinsGCT , CM000671.1:g.104184068_104184070delinsGCT GRCh37
NC_000009.10:g.103223889_103223891delinsGCT NCBI36
NG_012387.1:g.18993_18995delinsAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.*21_*23delinsAGC MANE Select ENSP00000497767.1:n.*21_*23delinsAGC
ENST00000648064.1:c.*21_*23delinsAGC ENSP00000497990.1:n.*21_*23delinsAGC
ENST00000648758.1:c.*21_*23delinsAGC ENSP00000497731.1:n.*21_*23delinsAGC
ENST00000374855.8:c.*21_*23delinsAGC ENSP00000363988.4:n.*21_*23delinsAGC
ENST00000616752.1:c.*128_*130delinsAGC ENSP00000481363.1:n.*128_*130delinsAGC
NM_000035.3:c.*21_*23delinsAGC NP_000026.2:n.*21_*23delinsAGC
NM_000035.4:c.*21_*23delinsAGC MANE Select NP_000026.2:n.*21_*23delinsAGC