Canonical Allele Identifier: CA868715373

Gene: FBP1

Linked Data

• dbSNP Id: rs1412980773
• gnomAD v4: 9-94639107-C-CA
• MyVariant Identifiers: chr9:g.97401389_97401390insA (hg19) ; chr9:g.94639107_94639108insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639108dup , CM000671.2:g.94639108dup	GRCh38
NC_000009.11:g.97401390dup , CM000671.1:g.97401390dup	GRCh37
NC_000009.10:g.96441211dup	NCBI36
NG_008174.1:g.6142dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+33dup	ENSP00000507547.1:n.170+33dup
ENST00000375326.9:c.170+33dup MANE Select	ENSP00000364475.5:n.170+33dup
ENST00000375326.8:c.170+33dup	ENSP00000364475.4:n.170+33dup
ENST00000414122.1:c.-83+936dup	ENSP00000411619.1:n.-83+936dup
ENST00000415431.5:c.170+33dup	ENSP00000408025.1:n.170+33dup
NM_000507.3:c.170+33dup	NP_000498.2:n.170+33dup
NM_001127628.1:c.170+33dup	NP_001121100.1:n.170+33dup
XM_006717005.2:c.-77+936dup	XP_006717068.1:n.-77+936dup
XM_006717005.4:c.-77+936dup	XP_006717068.1:n.-77+936dup
NM_000507.4:c.170+33dup MANE Select	NP_000498.2:n.170+33dup
NM_001127628.2:c.170+33dup	NP_001121100.1:n.170+33dup