Canonical Allele Identifier: CA1865226018
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605465T= , CM000671.2:g.94605465T= GRCh38
NC_000009.11:g.97367747T= , CM000671.1:g.97367747T= GRCh37
NC_000009.10:g.96407568T= NCBI36
NG_008174.1:g.39785A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.977A= ENSP00000507547.1:n.977A=
ENST00000375326.9:c.817A= MANE Select ENSP00000364475.5:p.Asn273=
ENST00000648117.1:c.622A= ENSP00000498145.1:p.Asn208=
ENST00000375326.8:c.817A= ENSP00000364475.4:p.Asn273=
ENST00000415431.5:c.817A= ENSP00000408025.1:p.Asn273=
NM_000507.3:c.817A= NP_000498.2:p.Asn273=
NM_001127628.1:c.817A= NP_001121100.1:p.Asn273=
XM_006717005.2:c.571A= XP_006717068.1:p.Asn191=
XM_006717005.4:c.571A= XP_006717068.1:p.Asn191=
NM_000507.4:c.817A= MANE Select NP_000498.2:p.Asn273=
NM_001127628.2:c.817A= NP_001121100.1:p.Asn273=