Canonical Allele Identifier: CA1865226063
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605555C= , CM000671.2:g.94605555C= GRCh38
NC_000009.11:g.97367837C= , CM000671.1:g.97367837C= GRCh37
NC_000009.10:g.96407658C= NCBI36
NG_008174.1:g.39695G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.887G= ENSP00000507547.1:n.887G=
ENST00000375326.9:c.727G= MANE Select ENSP00000364475.5:p.Ala243=
ENST00000648117.1:c.532G= ENSP00000498145.1:p.Ala178=
ENST00000375326.8:c.727G= ENSP00000364475.4:p.Ala243=
ENST00000415431.5:c.727G= ENSP00000408025.1:p.Ala243=
NM_000507.3:c.727G= NP_000498.2:p.Ala243=
NM_001127628.1:c.727G= NP_001121100.1:p.Ala243=
XM_006717005.2:c.481G= XP_006717068.1:p.Ala161=
XM_006717005.4:c.481G= XP_006717068.1:p.Ala161=
NM_000507.4:c.727G= MANE Select NP_000498.2:p.Ala243=
NM_001127628.2:c.727G= NP_001121100.1:p.Ala243=