Canonical Allele Identifier: CA589584189

Gene: FBP1

Linked Data

• dbSNP Id: rs1563991803
• gnomAD v2: 9-97401642-GGCTGCAGGTGCGGGCGGCAAGAGAGGGCAGTAGGCACTGGCCGCAGGTGCGGA-G
• gnomAD v3: 9-94639360-GGCTGCAGGTGCGGGCGGCAAGAGAGGGCAGTAGGCACTGGCCGCAGGTGCGGA-G
• gnomAD v4: 9-94639360-GGCTGCAGGTGCGGGCGGCAAGAGAGGGCAGTAGGCACTGGCCGCAGGTGCGGA-G
• MyVariant Identifiers: chr9:g.97401643_97401695del (hg19) ; chr9:g.94639361_94639413del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639380_94639432del , CM000671.2:g.94639380_94639432del	GRCh38
NC_000009.11:g.97401662_97401714del , CM000671.1:g.97401662_97401714del	GRCh37
NC_000009.10:g.96441483_96441535del	NCBI36
NG_008174.1:g.5837_5889del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-103_-51del MANE Select	ENSP00000364475.5:n.-103_-51del
ENST00000375326.8:c.-103_-51del	ENSP00000364475.4:n.-103_-51del
ENST00000414122.1:c.-83+631_-83+683del	ENSP00000411619.1:n.-83+631_-83+683del
ENST00000415431.5:c.-24-79_-24-27del	ENSP00000408025.1:n.-24-79_-24-27del
NM_000507.3:c.-103_-51del	NP_000498.2:n.-103_-51del
NM_001127628.1:c.-24-79_-24-27del	NP_001121100.1:n.-24-79_-24-27del
XM_006717005.2:c.-77+631_-77+683del	XP_006717068.1:n.-77+631_-77+683del
XM_006717005.4:c.-77+631_-77+683del	XP_006717068.1:n.-77+631_-77+683del
NM_000507.4:c.-103_-51del MANE Select	NP_000498.2:n.-103_-51del
NM_001127628.2:c.-24-79_-24-27del	NP_001121100.1:n.-24-79_-24-27del