Canonical Allele Identifier: CA1865226632
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94606849A= , CM000671.2:g.94606849A= GRCh38
NC_000009.11:g.97369131A= , CM000671.1:g.97369131A= GRCh37
NC_000009.10:g.96408952A= NCBI36
NG_008174.1:g.38401T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.831T= ENSP00000507547.1:n.831T=
ENST00000375326.9:c.671T= MANE Select ENSP00000364475.5:p.Val224=
ENST00000648117.1:c.476T= ENSP00000498145.1:p.Val159=
ENST00000375326.8:c.671T= ENSP00000364475.4:p.Val224=
ENST00000414122.1:c.419T= ENSP00000411619.1:p.Val140=
ENST00000415431.5:c.671T= ENSP00000408025.1:p.Val224=
NM_000507.3:c.671T= NP_000498.2:p.Val224=
NM_001127628.1:c.671T= NP_001121100.1:p.Val224=
XM_006717005.2:c.425T= XP_006717068.1:p.Val142=
XM_006717005.4:c.425T= XP_006717068.1:p.Val142=
NM_000507.4:c.671T= MANE Select NP_000498.2:p.Val224=
NM_001127628.2:c.671T= NP_001121100.1:p.Val224=