Canonical Allele Identifier: CA1865226020
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94605466G= , CM000671.2:g.94605466G= GRCh38
NC_000009.11:g.97367748G= , CM000671.1:g.97367748G= GRCh37
NC_000009.10:g.96407569G= NCBI36
NG_008174.1:g.39784C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.976C= ENSP00000507547.1:n.976C=
ENST00000375326.9:c.816C= MANE Select ENSP00000364475.5:p.Pro272=
ENST00000648117.1:c.621C= ENSP00000498145.1:p.Pro207=
ENST00000375326.8:c.816C= ENSP00000364475.4:p.Pro272=
ENST00000415431.5:c.816C= ENSP00000408025.1:p.Pro272=
NM_000507.3:c.816C= NP_000498.2:p.Pro272=
NM_001127628.1:c.816C= NP_001121100.1:p.Pro272=
XM_006717005.2:c.570C= XP_006717068.1:p.Pro190=
XM_006717005.4:c.570C= XP_006717068.1:p.Pro190=
NM_000507.4:c.816C= MANE Select NP_000498.2:p.Pro272=
NM_001127628.2:c.816C= NP_001121100.1:p.Pro272=