Canonical Allele Identifier: CA196571905

Gene: FBP1

Linked Data

• dbSNP Id: rs558159759
• gnomAD v3: 9-94638998-CAGAG-C
• gnomAD v4: 9-94638998-CAGAG-C
• MyVariant Identifiers: chr9:g.97401281_97401284del (hg19) ; chr9:g.94638999_94639002del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639001_94639004del , CM000671.2:g.94639001_94639004del	GRCh38
NC_000009.11:g.97401283_97401286del , CM000671.1:g.97401283_97401286del	GRCh37
NC_000009.10:g.96441104_96441107del	NCBI36
NG_008174.1:g.6248_6251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+139_170+142del	ENSP00000507547.1:n.170+139_170+142del
ENST00000375326.9:c.170+139_170+142del MANE Select	ENSP00000364475.5:n.170+139_170+142del
ENST00000375326.8:c.170+139_170+142del	ENSP00000364475.4:n.170+139_170+142del
ENST00000414122.1:c.-83+1042_-83+1045del	ENSP00000411619.1:n.-83+1042_-83+1045del
ENST00000415431.5:c.170+139_170+142del	ENSP00000408025.1:n.170+139_170+142del
NM_000507.3:c.170+139_170+142del	NP_000498.2:n.170+139_170+142del
NM_001127628.1:c.170+139_170+142del	NP_001121100.1:n.170+139_170+142del
XM_006717005.2:c.-77+1042_-77+1045del	XP_006717068.1:n.-77+1042_-77+1045del
XM_006717005.4:c.-77+1042_-77+1045del	XP_006717068.1:n.-77+1042_-77+1045del
NM_000507.4:c.170+139_170+142del MANE Select	NP_000498.2:n.170+139_170+142del
NM_001127628.2:c.170+139_170+142del	NP_001121100.1:n.170+139_170+142del