Canonical Allele Identifier: CA1865265130
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639191T= , CM000671.2:g.94639191T= GRCh38
NC_000009.11:g.97401473T= , CM000671.1:g.97401473T= GRCh37
NC_000009.10:g.96441294T= NCBI36
NG_008174.1:g.6059A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.120A= ENSP00000507547.1:p.Thr40=
ENST00000375326.9:c.120A= MANE Select ENSP00000364475.5:p.Thr40=
ENST00000375326.8:c.120A= ENSP00000364475.4:p.Thr40=
ENST00000414122.1:c.-83+853A= ENSP00000411619.1:n.-83+853A=
ENST00000415431.5:c.120A= ENSP00000408025.1:p.Thr40=
NM_000507.3:c.120A= NP_000498.2:p.Thr40=
NM_001127628.1:c.120A= NP_001121100.1:p.Thr40=
XM_006717005.2:c.-77+853A= XP_006717068.1:n.-77+853A=
XM_006717005.4:c.-77+853A= XP_006717068.1:n.-77+853A=
NM_000507.4:c.120A= MANE Select NP_000498.2:p.Thr40=
NM_001127628.2:c.120A= NP_001121100.1:p.Thr40=