Canonical Allele Identifier: CA2565156084
Gene: ALDOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425570_101425572del , CM000671.2:g.101425570_101425572del GRCh38
NC_000009.11:g.104187852_104187854del , CM000671.1:g.104187852_104187854del GRCh37
NC_000009.10:g.103227673_103227675del NCBI36
NG_012387.1:g.15209_15211del

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.680_682del MANE Select ENSP00000497767.1:p.Thr227_Leu228delinsMe...
ENST00000648064.1:c.680_682del ENSP00000497990.1:p.Thr227_Leu228delinsMe...
ENST00000648758.1:c.680_682del ENSP00000497731.1:p.Thr227_Leu228delinsMe...
ENST00000649902.1:c.680_682del ENSP00000497216.1:p.Thr227_Leu228delinsMe...
ENST00000374855.8:c.680_682del ENSP00000363988.4:p.Thr227_Leu228delinsMe...
ENST00000468981.3:n.207_209del
ENST00000616752.1:c.680_682del ENSP00000481363.1:p.Thr227_Leu228delinsMe...
NM_000035.3:c.680_682del NP_000026.2:p.Thr227_Leu228delinsMet
NM_000035.4:c.680_682del MANE Select NP_000026.2:p.Thr227_Leu228delinsMet