Canonical Allele Identifier: CA5136376

Gene: FBP1

Linked Data

• dbSNP Id: rs764449536
• ExAC: 9:97401628 A / AGCGGCAGGTGCGGG
• gnomAD v2: 9-97401628-A-AGCGGCAGGTGCGGG
• gnomAD v3: 9-94639346-A-AGCGGCAGGTGCGGG
• gnomAD v4: 9-94639346-A-AGCGGCAGGTGCGGG
• MyVariant Identifiers: chr9:g.97401628_97401629insGCGGCAGGTGCGGG (hg19) ; chr9:g.94639346_94639347insGCGGCAGGTGCGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639349_94639362dup , CM000671.2:g.94639349_94639362dup	GRCh38
NC_000009.11:g.97401631_97401644dup , CM000671.1:g.97401631_97401644dup	GRCh37
NC_000009.10:g.96441452_96441465dup	NCBI36
NG_008174.1:g.5890_5903dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-50_-37dup MANE Select	ENSP00000364475.5:n.-50_-37dup
ENST00000375326.8:c.-50_-37dup	ENSP00000364475.4:n.-50_-37dup
ENST00000414122.1:c.-83+684_-83+697dup	ENSP00000411619.1:n.-83+684_-83+697dup
ENST00000415431.5:c.-24-26_-24-13dup	ENSP00000408025.1:n.-24-26_-24-13dup
NM_000507.3:c.-50_-37dup	NP_000498.2:n.-50_-37dup
NM_001127628.1:c.-24-26_-24-13dup	NP_001121100.1:n.-24-26_-24-13dup
XM_006717005.2:c.-77+684_-77+697dup	XP_006717068.1:n.-77+684_-77+697dup
XM_006717005.4:c.-77+684_-77+697dup	XP_006717068.1:n.-77+684_-77+697dup
NM_000507.4:c.-50_-37dup MANE Select	NP_000498.2:n.-50_-37dup
NM_001127628.2:c.-24-26_-24-13dup	NP_001121100.1:n.-24-26_-24-13dup