Canonical Allele Identifier: CA1865264997

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639094_94639098delinsCCAGG , CM000671.2:g.94639094_94639098delinsCCAGG	GRCh38
NC_000009.11:g.97401376_97401380delinsCCAGG , CM000671.1:g.97401376_97401380delinsCCAGG	GRCh37
NC_000009.10:g.96441197_96441201delinsCCAGG	NCBI36
NG_008174.1:g.6152_6156delinsCCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+43_170+47delinsCCTGG	ENSP00000507547.1:n.170+43_170+47delinsCCTGG
ENST00000375326.9:c.170+43_170+47delinsCCTGG MANE Select	ENSP00000364475.5:n.170+43_170+47delinsCCTGG
ENST00000375326.8:c.170+43_170+47delinsCCTGG	ENSP00000364475.4:n.170+43_170+47delinsCCTGG
ENST00000414122.1:c.-83+946_-83+950delinsCCTGG	ENSP00000411619.1:n.-83+946_-83+950delinsCCTGG
ENST00000415431.5:c.170+43_170+47delinsCCTGG	ENSP00000408025.1:n.170+43_170+47delinsCCTGG
NM_000507.3:c.170+43_170+47delinsCCTGG	NP_000498.2:n.170+43_170+47delinsCCTGG
NM_001127628.1:c.170+43_170+47delinsCCTGG	NP_001121100.1:n.170+43_170+47delinsCCTGG
XM_006717005.2:c.-77+946_-77+950delinsCCTGG	XP_006717068.1:n.-77+946_-77+950delinsCCTGG
XM_006717005.4:c.-77+946_-77+950delinsCCTGG	XP_006717068.1:n.-77+946_-77+950delinsCCTGG
NM_000507.4:c.170+43_170+47delinsCCTGG MANE Select	NP_000498.2:n.170+43_170+47delinsCCTGG
NM_001127628.2:c.170+43_170+47delinsCCTGG	NP_001121100.1:n.170+43_170+47delinsCCTGG