Canonical Allele Identifier: CA2690771539
Gene: FBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639441_94639442insAGTAGG , CM000671.2:g.94639441_94639442insAGTAGG GRCh38
NC_000009.11:g.97401723_97401724insAGTAGG , CM000671.1:g.97401723_97401724insAGTAGG GRCh37
NC_000009.10:g.96441544_96441545insAGTAGG NCBI36
NG_008174.1:g.5808_5809insCCTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-132_-131insCCTACT MANE Select ENSP00000364475.5:n.-132_-131insCCTACT
ENST00000375326.8:c.-132_-131insCCTACT ENSP00000364475.4:n.-132_-131insCCTACT
ENST00000414122.1:c.-83+602_-83+603insCCTACT ENSP00000411619.1:n.-83+602_-83+603insCCTACT
ENST00000415431.5:c.-24-108_-24-107insCCTACT ENSP00000408025.1:n.-24-108_-24-107insCCTACT
NM_000507.3:c.-132_-131insCCTACT NP_000498.2:n.-132_-131insCCTACT
NM_001127628.1:c.-24-108_-24-107insCCTACT NP_001121100.1:n.-24-108_-24-107insCCTACT
XM_006717005.2:c.-77+602_-77+603insCCTACT XP_006717068.1:n.-77+602_-77+603insCCTACT
XM_006717005.4:c.-77+602_-77+603insCCTACT XP_006717068.1:n.-77+602_-77+603insCCTACT
NM_000507.4:c.-132_-131insCCTACT MANE Select NP_000498.2:n.-132_-131insCCTACT
NM_001127628.2:c.-24-108_-24-107insCCTACT NP_001121100.1:n.-24-108_-24-107insCCTACT