Canonical Allele Identifier: CA1865265098
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94639169C= , CM000671.2:g.94639169C= GRCh38
NC_000009.11:g.97401451C= , CM000671.1:g.97401451C= GRCh37
NC_000009.10:g.96441272C= NCBI36
NG_008174.1:g.6081G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.142G= ENSP00000507547.1:p.Ala48=
ENST00000375326.9:c.142G= MANE Select ENSP00000364475.5:p.Ala48=
ENST00000375326.8:c.142G= ENSP00000364475.4:p.Ala48=
ENST00000414122.1:c.-83+875G= ENSP00000411619.1:n.-83+875G=
ENST00000415431.5:c.142G= ENSP00000408025.1:p.Ala48=
NM_000507.3:c.142G= NP_000498.2:p.Ala48=
NM_001127628.1:c.142G= NP_001121100.1:p.Ala48=
XM_006717005.2:c.-77+875G= XP_006717068.1:n.-77+875G=
XM_006717005.4:c.-77+875G= XP_006717068.1:n.-77+875G=
NM_000507.4:c.142G= MANE Select NP_000498.2:p.Ala48=
NM_001127628.2:c.142G= NP_001121100.1:p.Ala48=