Canonical Allele Identifier: CA5136371

Gene: FBP1

Linked Data

• dbSNP Id: rs758509921
• ExAC: 9:97401610 CGCGGGGCTGCAGGTGCAAGCGGCAGGT / C
• gnomAD v2: 9-97401610-CGCGGGGCTGCAGGTGCAAGCGGCAGGT-C
• gnomAD v3: 9-94639328-CGCGGGGCTGCAGGTGCAAGCGGCAGGT-C
• gnomAD v4: 9-94639328-CGCGGGGCTGCAGGTGCAAGCGGCAGGT-C
• MyVariant Identifiers: chr9:g.97401611_97401637del (hg19) ; chr9:g.94639329_94639355del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639345_94639371del , CM000671.2:g.94639345_94639371del	GRCh38
NC_000009.11:g.97401627_97401653del , CM000671.1:g.97401627_97401653del	GRCh37
NC_000009.10:g.96441448_96441474del	NCBI36
NG_008174.1:g.5895_5921del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375326.9:c.-45_-19del MANE Select	ENSP00000364475.5:n.-45_-19del
ENST00000375326.8:c.-45_-19del	ENSP00000364475.4:n.-45_-19del
ENST00000414122.1:c.-83+689_-83+715del	ENSP00000411619.1:n.-83+689_-83+715del
ENST00000415431.5:c.-24-21_-19del
NM_000507.3:c.-45_-19del	NP_000498.2:n.-45_-19del
NM_001127628.1:c.-24-21_-19del
XM_006717005.2:c.-77+689_-77+715del	XP_006717068.1:n.-77+689_-77+715del
XM_006717005.4:c.-77+689_-77+715del	XP_006717068.1:n.-77+689_-77+715del
NM_000507.4:c.-45_-19del MANE Select	NP_000498.2:n.-45_-19del
NM_001127628.2:c.-24-21_-19del