Canonical Allele Identifier: CA2690769534
Gene: FBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94609910del , CM000671.2:g.94609910del GRCh38
NC_000009.11:g.97372192del , CM000671.1:g.97372192del GRCh37
NC_000009.10:g.96412013del NCBI36
NG_008174.1:g.35340del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.567+11del ENSP00000507547.1:n.567+11del
ENST00000375326.9:c.567+11del MANE Select ENSP00000364475.5:n.567+11del
ENST00000648117.1:c.372+11del ENSP00000498145.1:n.372+11del
ENST00000375326.8:c.567+11del ENSP00000364475.4:n.567+11del
ENST00000414122.1:c.315+11del ENSP00000411619.1:n.315+11del
ENST00000415431.5:c.567+11del ENSP00000408025.1:n.567+11del
NM_000507.3:c.567+11del NP_000498.2:n.567+11del
NM_001127628.1:c.567+11del NP_001121100.1:n.567+11del
XM_006717005.2:c.321+11del XP_006717068.1:n.321+11del
XM_006717005.4:c.321+11del XP_006717068.1:n.321+11del
NM_000507.4:c.567+11del MANE Select NP_000498.2:n.567+11del
NM_001127628.2:c.567+11del NP_001121100.1:n.567+11del