Canonical Allele Identifier: CA1865225069
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94603348A= , CM000671.2:g.94603348A= GRCh38
NC_000009.11:g.97365630A= , CM000671.1:g.97365630A= GRCh37
NC_000009.10:g.96405451A= NCBI36
NG_008174.1:g.41902T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.1210T= ENSP00000507547.1:n.1210T=
ENST00000375326.9:c.*33T= MANE Select ENSP00000364475.5:n.*33T=
ENST00000648117.1:c.*33T= ENSP00000498145.1:n.*33T=
ENST00000375326.8:c.*33T= ENSP00000364475.4:n.*33T=
ENST00000415431.5:c.*33T= ENSP00000408025.1:n.*33T=
NM_000507.3:c.*33T= NP_000498.2:n.*33T=
NM_001127628.1:c.*33T= NP_001121100.1:n.*33T=
XM_006717005.2:c.*33T= XP_006717068.1:n.*33T=
XM_006717005.4:c.*33T= XP_006717068.1:n.*33T=
NM_000507.4:c.*33T= MANE Select NP_000498.2:n.*33T=
NM_001127628.2:c.*33T= NP_001121100.1:n.*33T=