Canonical Allele Identifier: CA2695210730
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639277del , CM000671.2:g.94639277del GRCh38
NC_000009.11:g.97401559del , CM000671.1:g.97401559del GRCh37
NC_000009.10:g.96441380del NCBI36
NG_008174.1:g.5974del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.35del ENSP00000507547.1:p.Asn12ThrfsTer3
ENST00000375326.9:c.35del MANE Select ENSP00000364475.5:p.Asn12ThrfsTer3
ENST00000375326.8:c.35del ENSP00000364475.4:p.Asn12ThrfsTer3
ENST00000414122.1:c.-83+768del ENSP00000411619.1:n.-83+768del
ENST00000415431.5:c.35del ENSP00000408025.1:p.Asn12ThrfsTer3
NM_000507.3:c.35del NP_000498.2:p.Asn12ThrfsTer3
NM_001127628.1:c.35del NP_001121100.1:p.Asn12ThrfsTer3
XM_006717005.2:c.-77+768del XP_006717068.1:n.-77+768del
XM_006717005.4:c.-77+768del XP_006717068.1:n.-77+768del
NM_000507.4:c.35del MANE Select NP_000498.2:p.Asn12ThrfsTer3
NM_001127628.2:c.35del NP_001121100.1:p.Asn12ThrfsTer3