Canonical Allele Identifier: CA2579387201
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605365del , CM000671.2:g.94605365del GRCh38
NC_000009.11:g.97367647del , CM000671.1:g.97367647del GRCh37
NC_000009.10:g.96407468del NCBI36
NG_008174.1:g.39886del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.985+93del ENSP00000507547.1:n.985+93del
ENST00000375326.9:c.825+93del MANE Select ENSP00000364475.5:n.825+93del
ENST00000648117.1:c.630+93del ENSP00000498145.1:n.630+93del
ENST00000375326.8:c.825+93del ENSP00000364475.4:n.825+93del
ENST00000415431.5:c.825+93del ENSP00000408025.1:n.825+93del
NM_000507.3:c.825+93del NP_000498.2:n.825+93del
NM_001127628.1:c.825+93del NP_001121100.1:n.825+93del
XM_006717005.2:c.579+93del XP_006717068.1:n.579+93del
XM_006717005.4:c.579+93del XP_006717068.1:n.579+93del
NM_000507.4:c.825+93del MANE Select NP_000498.2:n.825+93del
NM_001127628.2:c.825+93del NP_001121100.1:n.825+93del