Canonical Allele Identifier: CA2690769176
Gene: FBP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605557_94605558dup , CM000671.2:g.94605557_94605558dup GRCh38
NC_000009.11:g.97367839_97367840dup , CM000671.1:g.97367839_97367840dup GRCh37
NC_000009.10:g.96407660_96407661dup NCBI36
NG_008174.1:g.39694_39695dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.886_887dup ENSP00000507547.1:n.886_887dup
ENST00000375326.9:c.726_727dup MANE Select ENSP00000364475.5:p.Ala243GlyfsTer?
ENST00000648117.1:c.531_532dup ENSP00000498145.1:p.Ala178GlyfsTer?
ENST00000375326.8:c.726_727dup ENSP00000364475.4:p.Ala243GlyfsTer?
ENST00000415431.5:c.726_727dup ENSP00000408025.1:p.Ala243GlyfsTer?
NM_000507.3:c.726_727dup NP_000498.2:p.Ala243GlyfsTer?
NM_001127628.1:c.726_727dup NP_001121100.1:p.Ala243GlyfsTer?
XM_006717005.2:c.480_481dup XP_006717068.1:p.Ala161GlyfsTer?
XM_006717005.4:c.480_481dup XP_006717068.1:p.Ala161GlyfsTer?
NM_000507.4:c.726_727dup MANE Select NP_000498.2:p.Ala243GlyfsTer?
NM_001127628.2:c.726_727dup NP_001121100.1:p.Ala243GlyfsTer?