Canonical Allele Identifier: CA16609828
Gene: FBP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403701
ClinVar RCV Id: RCV000456113
dbSNP Id: rs1060499726
MyVariant Identifiers: chr9:g.97367835_97367844del (hg19) chr9:g.94605553_94605562del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605555_94605564del , CM000671.2:g.94605555_94605564del GRCh38
NC_000009.11:g.97367837_97367846del , CM000671.1:g.97367837_97367846del GRCh37
NC_000009.10:g.96407658_96407667del NCBI36
NG_008174.1:g.39688_39697del

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.880_889del ENSP00000507547.1:n.880_889del
ENST00000375326.9:c.720_729del MANE Select ENSP00000364475.5:p.Tyr241GlyfsTer?
ENST00000648117.1:c.525_534del ENSP00000498145.1:p.Tyr176GlyfsTer?
ENST00000375326.8:c.720_729del ENSP00000364475.4:p.Tyr241GlyfsTer?
ENST00000415431.5:c.720_729del ENSP00000408025.1:p.Tyr241GlyfsTer?
NM_000507.3:c.720_729del NP_000498.2:p.Tyr241GlyfsTer?
NM_001127628.1:c.720_729del NP_001121100.1:p.Tyr241GlyfsTer?
XM_006717005.2:c.474_483del XP_006717068.1:p.Tyr159GlyfsTer?
XM_006717005.4:c.474_483del XP_006717068.1:p.Tyr159GlyfsTer?
NM_000507.4:c.720_729del MANE Select NP_000498.2:p.Tyr241GlyfsTer?
NM_001127628.2:c.720_729del NP_001121100.1:p.Tyr241GlyfsTer?
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