Canonical Allele Identifier: CA1865228017
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94610006A= , CM000671.2:g.94610006A= GRCh38
NC_000009.11:g.97372288A= , CM000671.1:g.97372288A= GRCh37
NC_000009.10:g.96412109A= NCBI36
NG_008174.1:g.35244T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.482T= ENSP00000507547.1:p.Val161=
ENST00000375326.9:c.482T= MANE Select ENSP00000364475.5:p.Val161=
ENST00000648117.1:c.287T= ENSP00000498145.1:p.Val96=
ENST00000375326.8:c.482T= ENSP00000364475.4:p.Val161=
ENST00000414122.1:c.230T= ENSP00000411619.1:p.Val77=
ENST00000415431.5:c.482T= ENSP00000408025.1:p.Val161=
NM_000507.3:c.482T= NP_000498.2:p.Val161=
NM_001127628.1:c.482T= NP_001121100.1:p.Val161=
XM_006717005.2:c.236T= XP_006717068.1:p.Val79=
XM_006717005.4:c.236T= XP_006717068.1:p.Val79=
NM_000507.4:c.482T= MANE Select NP_000498.2:p.Val161=
NM_001127628.2:c.482T= NP_001121100.1:p.Val161=