Canonical Allele Identifier: CA1865226630
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94606843T= , CM000671.2:g.94606843T= GRCh38
NC_000009.11:g.97369125T= , CM000671.1:g.97369125T= GRCh37
NC_000009.10:g.96408946T= NCBI36
NG_008174.1:g.38407A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.837A= ENSP00000507547.1:n.837A=
ENST00000375326.9:c.677A= MANE Select ENSP00000364475.5:p.Glu226=
ENST00000648117.1:c.482A= ENSP00000498145.1:p.Glu161=
ENST00000375326.8:c.677A= ENSP00000364475.4:p.Glu226=
ENST00000414122.1:c.425A= ENSP00000411619.1:p.Glu142=
ENST00000415431.5:c.677A= ENSP00000408025.1:p.Glu226=
NM_000507.3:c.677A= NP_000498.2:p.Glu226=
NM_001127628.1:c.677A= NP_001121100.1:p.Glu226=
XM_006717005.2:c.431A= XP_006717068.1:p.Glu144=
XM_006717005.4:c.431A= XP_006717068.1:p.Glu144=
NM_000507.4:c.677A= MANE Select NP_000498.2:p.Glu226=
NM_001127628.2:c.677A= NP_001121100.1:p.Glu226=