Canonical Allele Identifier: CA1865265616
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639463_94639467delinsTGACA , CM000671.2:g.94639463_94639467delinsTGACA GRCh38
NC_000009.11:g.97401745_97401749delinsTGACA , CM000671.1:g.97401745_97401749delinsTGACA GRCh37
NC_000009.10:g.96441566_96441570delinsTGACA NCBI36
NG_008174.1:g.5783_5787delinsTGTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-157_-153delinsTGTCA MANE Select ENSP00000364475.5:n.-157_-153delinsTGTCA
ENST00000375326.8:c.-157_-153delinsTGTCA ENSP00000364475.4:n.-157_-153delinsTGTCA
ENST00000414122.1:c.-83+577_-83+581delinsTGTCA ENSP00000411619.1:n.-83+577_-83+581delinsTGTCA
ENST00000415431.5:c.-24-133_-24-129delinsTGTCA ENSP00000408025.1:n.-24-133_-24-129delinsTGTCA
NM_000507.3:c.-157_-153delinsTGTCA NP_000498.2:n.-157_-153delinsTGTCA
NM_001127628.1:c.-24-133_-24-129delinsTGTCA NP_001121100.1:n.-24-133_-24-129delinsTGTCA
XM_006717005.2:c.-77+577_-77+581delinsTGTCA XP_006717068.1:n.-77+577_-77+581delinsTGTCA
XM_006717005.4:c.-77+577_-77+581delinsTGTCA XP_006717068.1:n.-77+577_-77+581delinsTGTCA
NM_000507.4:c.-157_-153delinsTGTCA MANE Select NP_000498.2:n.-157_-153delinsTGTCA
NM_001127628.2:c.-24-133_-24-129delinsTGTCA NP_001121100.1:n.-24-133_-24-129delinsTGTCA