Canonical Allele Identifier: CA1865265626
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639465A= , CM000671.2:g.94639465A= GRCh38
NC_000009.11:g.97401747A= , CM000671.1:g.97401747A= GRCh37
NC_000009.10:g.96441568A= NCBI36
NG_008174.1:g.5785T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375326.9:c.-155T= MANE Select ENSP00000364475.5:n.-155T=
ENST00000375326.8:c.-155T= ENSP00000364475.4:n.-155T=
ENST00000414122.1:c.-83+579T= ENSP00000411619.1:n.-83+579T=
ENST00000415431.5:c.-24-131T= ENSP00000408025.1:n.-24-131T=
NM_000507.3:c.-155T= NP_000498.2:n.-155T=
NM_001127628.1:c.-24-131T= NP_001121100.1:n.-24-131T=
XM_006717005.2:c.-77+579T= XP_006717068.1:n.-77+579T=
XM_006717005.4:c.-77+579T= XP_006717068.1:n.-77+579T=
NM_000507.4:c.-155T= MANE Select NP_000498.2:n.-155T=
NM_001127628.2:c.-24-131T= NP_001121100.1:n.-24-131T=