Canonical Allele Identifier: CA868730022

Gene: FBP1

Linked Data

• dbSNP Id: rs1238982329
• gnomAD v3: 9-94609900-G-GC
• gnomAD v4: 9-94609900-G-GC
• MyVariant Identifiers: chr9:g.97372182_97372183insC (hg19) ; chr9:g.94609900_94609901insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94609902dup , CM000671.2:g.94609902dup	GRCh38
NC_000009.11:g.97372184dup , CM000671.1:g.97372184dup	GRCh37
NC_000009.10:g.96412005dup	NCBI36
NG_008174.1:g.35349dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.567+20dup	ENSP00000507547.1:n.567+20dup
ENST00000375326.9:c.567+20dup MANE Select	ENSP00000364475.5:n.567+20dup
ENST00000648117.1:c.372+20dup	ENSP00000498145.1:n.372+20dup
ENST00000375326.8:c.567+20dup	ENSP00000364475.4:n.567+20dup
ENST00000414122.1:c.315+20dup	ENSP00000411619.1:n.315+20dup
ENST00000415431.5:c.567+20dup	ENSP00000408025.1:n.567+20dup
NM_000507.3:c.567+20dup	NP_000498.2:n.567+20dup
NM_001127628.1:c.567+20dup	NP_001121100.1:n.567+20dup
XM_006717005.2:c.321+20dup	XP_006717068.1:n.321+20dup
XM_006717005.4:c.321+20dup	XP_006717068.1:n.321+20dup
NM_000507.4:c.567+20dup MANE Select	NP_000498.2:n.567+20dup
NM_001127628.2:c.567+20dup	NP_001121100.1:n.567+20dup