Canonical Allele Identifier: CA1865264774
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94638864A= , CM000671.2:g.94638864A= GRCh38
NC_000009.11:g.97401146A= , CM000671.1:g.97401146A= GRCh37
NC_000009.10:g.96440967A= NCBI36
NG_008174.1:g.6386T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.170+277T= ENSP00000507547.1:n.170+277T=
ENST00000375326.9:c.170+277T= MANE Select ENSP00000364475.5:n.170+277T=
ENST00000375326.8:c.170+277T= ENSP00000364475.4:n.170+277T=
ENST00000414122.1:c.-83+1180T= ENSP00000411619.1:n.-83+1180T=
ENST00000415431.5:c.170+277T= ENSP00000408025.1:n.170+277T=
NM_000507.3:c.170+277T= NP_000498.2:n.170+277T=
NM_001127628.1:c.170+277T= NP_001121100.1:n.170+277T=
XM_006717005.2:c.-77+1180T= XP_006717068.1:n.-77+1180T=
XM_006717005.4:c.-77+1180T= XP_006717068.1:n.-77+1180T=
NM_000507.4:c.170+277T= MANE Select NP_000498.2:n.170+277T=
NM_001127628.2:c.170+277T= NP_001121100.1:n.170+277T=