Canonical Allele Identifier: CA1865240006
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94620408A= , CM000671.2:g.94620408A= GRCh38
NC_000009.11:g.97382690A= , CM000671.1:g.97382690A= GRCh37
NC_000009.10:g.96422511A= NCBI36
NG_008174.1:g.24842T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.254T= ENSP00000507547.1:p.Met85=
ENST00000375326.9:c.254T= MANE Select ENSP00000364475.5:p.Met85=
ENST00000648117.1:c.152T= ENSP00000498145.1:p.Met51=
ENST00000375326.8:c.254T= ENSP00000364475.4:p.Met85=
ENST00000414122.1:c.2T= ENSP00000411619.1:p.Met1=
ENST00000415431.5:c.254T= ENSP00000408025.1:p.Met85=
NM_000507.3:c.254T= NP_000498.2:p.Met85=
NM_001127628.1:c.254T= NP_001121100.1:p.Met85=
XM_006717005.2:c.8T= XP_006717068.1:p.Met3=
XM_006717005.4:c.8T= XP_006717068.1:p.Met3=
NM_000507.4:c.254T= MANE Select NP_000498.2:p.Met85=
NM_001127628.2:c.254T= NP_001121100.1:p.Met85=