Canonical Allele Identifier: CA2690769956

Gene: FBP1

Linked Data

• gnomAD v4: 9-94639346-AGCGGCAGGTGCGGGGCTGCAGGTGCGGGCGGCAAGAGAGGGCAGTAGGCACTGGCCGCAGGTGCGGAGCTGCAGGTGCGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639361_94639440del , CM000671.2:g.94639361_94639440del	GRCh38
NC_000009.11:g.97401643_97401722del , CM000671.1:g.97401643_97401722del	GRCh37
NC_000009.10:g.96441464_96441543del	NCBI36
NG_008174.1:g.5824_5903del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-116_-37del MANE Select	ENSP00000364475.5:n.-116_-37del
ENST00000375326.8:c.-116_-37del	ENSP00000364475.4:n.-116_-37del
ENST00000414122.1:c.-83+618_-83+697del	ENSP00000411619.1:n.-83+618_-83+697del
ENST00000415431.5:c.-24-92_-24-13del	ENSP00000408025.1:n.-24-92_-24-13del
NM_000507.3:c.-116_-37del	NP_000498.2:n.-116_-37del
NM_001127628.1:c.-24-92_-24-13del	NP_001121100.1:n.-24-92_-24-13del
XM_006717005.2:c.-77+618_-77+697del	XP_006717068.1:n.-77+618_-77+697del
XM_006717005.4:c.-77+618_-77+697del	XP_006717068.1:n.-77+618_-77+697del
NM_000507.4:c.-116_-37del MANE Select	NP_000498.2:n.-116_-37del
NM_001127628.2:c.-24-92_-24-13del	NP_001121100.1:n.-24-92_-24-13del