Canonical Allele Identifier: CA1865228018
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94610010G= , CM000671.2:g.94610010G= GRCh38
NC_000009.11:g.97372292G= , CM000671.1:g.97372292G= GRCh37
NC_000009.10:g.96412113G= NCBI36
NG_008174.1:g.35240C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682520.1:c.478C= ENSP00000507547.1:p.Leu160=
ENST00000375326.9:c.478C= MANE Select ENSP00000364475.5:p.Leu160=
ENST00000648117.1:c.283C= ENSP00000498145.1:p.Leu95=
ENST00000375326.8:c.478C= ENSP00000364475.4:p.Leu160=
ENST00000414122.1:c.226C= ENSP00000411619.1:p.Leu76=
ENST00000415431.5:c.478C= ENSP00000408025.1:p.Leu160=
NM_000507.3:c.478C= NP_000498.2:p.Leu160=
NM_001127628.1:c.478C= NP_001121100.1:p.Leu160=
XM_006717005.2:c.232C= XP_006717068.1:p.Leu78=
XM_006717005.4:c.232C= XP_006717068.1:p.Leu78=
NM_000507.4:c.478C= MANE Select NP_000498.2:p.Leu160=
NM_001127628.2:c.478C= NP_001121100.1:p.Leu160=