Canonical Allele Identifier: CA1865265561

Gene: FBP1

Linked Data

• dbSNP Id: rs1828251606
• gnomAD v4: 9-94639426-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639426_94639427insA , CM000671.2:g.94639426_94639427insA	GRCh38
NC_000009.11:g.97401708_97401709insA , CM000671.1:g.97401708_97401709insA	GRCh37
NC_000009.10:g.96441529_96441530insA	NCBI36
NG_008174.1:g.5823_5824insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-117_-116insT MANE Select	ENSP00000364475.5:n.-117_-116insT
ENST00000375326.8:c.-117_-116insT	ENSP00000364475.4:n.-117_-116insT
ENST00000414122.1:c.-83+617_-83+618insT	ENSP00000411619.1:n.-83+617_-83+618insT
ENST00000415431.5:c.-24-93_-24-92insT	ENSP00000408025.1:n.-24-93_-24-92insT
NM_000507.3:c.-117_-116insT	NP_000498.2:n.-117_-116insT
NM_001127628.1:c.-24-93_-24-92insT	NP_001121100.1:n.-24-93_-24-92insT
XM_006717005.2:c.-77+617_-77+618insT	XP_006717068.1:n.-77+617_-77+618insT
XM_006717005.4:c.-77+617_-77+618insT	XP_006717068.1:n.-77+617_-77+618insT
NM_000507.4:c.-117_-116insT MANE Select	NP_000498.2:n.-117_-116insT
NM_001127628.2:c.-24-93_-24-92insT	NP_001121100.1:n.-24-93_-24-92insT