Canonical Allele Identifier: CA589584207

Gene: FBP1

Linked Data

• dbSNP Id: rs1479569931
• gnomAD v2: 9-97401618-T-TGCAGGTGCAAGCG
• gnomAD v3: 9-94639336-T-TGCAGGTGCAAGCG
• gnomAD v4: 9-94639336-T-TGCAGGTGCAAGCG
• MyVariant Identifiers: chr9:g.97401618_97401619insGCAGGTGCAAGCG (hg19) ; chr9:g.94639336_94639337insGCAGGTGCAAGCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639345_94639357dup , CM000671.2:g.94639345_94639357dup	GRCh38
NC_000009.11:g.97401627_97401639dup , CM000671.1:g.97401627_97401639dup	GRCh37
NC_000009.10:g.96441448_96441460dup	NCBI36
NG_008174.1:g.5901_5913dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-39_-27dup MANE Select	ENSP00000364475.5:n.-39_-27dup
ENST00000375326.8:c.-39_-27dup	ENSP00000364475.4:n.-39_-27dup
ENST00000414122.1:c.-83+695_-83+707dup	ENSP00000411619.1:n.-83+695_-83+707dup
ENST00000415431.5:c.-24-15_-24-3dup	ENSP00000408025.1:n.-24-15_-24-3dup
NM_000507.3:c.-39_-27dup	NP_000498.2:n.-39_-27dup
NM_001127628.1:c.-24-15_-24-3dup	NP_001121100.1:n.-24-15_-24-3dup
XM_006717005.2:c.-77+695_-77+707dup	XP_006717068.1:n.-77+695_-77+707dup
XM_006717005.4:c.-77+695_-77+707dup	XP_006717068.1:n.-77+695_-77+707dup
NM_000507.4:c.-39_-27dup MANE Select	NP_000498.2:n.-39_-27dup
NM_001127628.2:c.-24-15_-24-3dup	NP_001121100.1:n.-24-15_-24-3dup