Canonical Allele Identifier: CA196571970

Gene: FBP1

Linked Data

• dbSNP Id: rs540596576
• gnomAD v2: 9-97401341-CAGAGGG-C
• gnomAD v3: 9-94639059-CAGAGGG-C
• gnomAD v4: 9-94639059-CAGAGGG-C
• MyVariant Identifiers: chr9:g.97401342_97401347del (hg19) ; chr9:g.94639060_94639065del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639060_94639065del , CM000671.2:g.94639060_94639065del	GRCh38
NC_000009.11:g.97401342_97401347del , CM000671.1:g.97401342_97401347del	GRCh37
NC_000009.10:g.96441163_96441168del	NCBI36
NG_008174.1:g.6185_6190del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+76_170+81del	ENSP00000507547.1:n.170+76_170+81del
ENST00000375326.9:c.170+76_170+81del MANE Select	ENSP00000364475.5:n.170+76_170+81del
ENST00000375326.8:c.170+76_170+81del	ENSP00000364475.4:n.170+76_170+81del
ENST00000414122.1:c.-83+979_-83+984del	ENSP00000411619.1:n.-83+979_-83+984del
ENST00000415431.5:c.170+76_170+81del	ENSP00000408025.1:n.170+76_170+81del
NM_000507.3:c.170+76_170+81del	NP_000498.2:n.170+76_170+81del
NM_001127628.1:c.170+76_170+81del	NP_001121100.1:n.170+76_170+81del
XM_006717005.2:c.-77+979_-77+984del	XP_006717068.1:n.-77+979_-77+984del
XM_006717005.4:c.-77+979_-77+984del	XP_006717068.1:n.-77+979_-77+984del
NM_000507.4:c.170+76_170+81del MANE Select	NP_000498.2:n.170+76_170+81del
NM_001127628.2:c.170+76_170+81del	NP_001121100.1:n.170+76_170+81del