Canonical Allele Identifier: CA2690771552
Gene: FBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639456_94639484del , CM000671.2:g.94639456_94639484del GRCh38
NC_000009.11:g.97401738_97401766del , CM000671.1:g.97401738_97401766del GRCh37
NC_000009.10:g.96441559_96441587del NCBI36
NG_008174.1:g.5768_5796del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-172_-144del MANE Select ENSP00000364475.5:n.-172_-144del
ENST00000375326.8:c.-172_-144del ENSP00000364475.4:n.-172_-144del
ENST00000414122.1:c.-83+562_-83+590del ENSP00000411619.1:n.-83+562_-83+590del
ENST00000415431.5:c.-24-148_-24-120del ENSP00000408025.1:n.-24-148_-24-120del
NM_000507.3:c.-172_-144del NP_000498.2:n.-172_-144del
NM_001127628.1:c.-24-148_-24-120del NP_001121100.1:n.-24-148_-24-120del
XM_006717005.2:c.-77+562_-77+590del XP_006717068.1:n.-77+562_-77+590del
XM_006717005.4:c.-77+562_-77+590del XP_006717068.1:n.-77+562_-77+590del
NM_000507.4:c.-172_-144del MANE Select NP_000498.2:n.-172_-144del
NM_001127628.2:c.-24-148_-24-120del NP_001121100.1:n.-24-148_-24-120del