Canonical Allele Identifier: CA1865225182
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94603549G= , CM000671.2:g.94603549G= GRCh38
NC_000009.11:g.97365831G= , CM000671.1:g.97365831G= GRCh37
NC_000009.10:g.96405652G= NCBI36
NG_008174.1:g.41701C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.1009C= ENSP00000507547.1:n.1009C=
ENST00000375326.9:c.849C= MANE Select ENSP00000364475.5:p.Asn283=
ENST00000648117.1:c.654C= ENSP00000498145.1:p.Asn218=
ENST00000375326.8:c.849C= ENSP00000364475.4:p.Asn283=
ENST00000415431.5:c.849C= ENSP00000408025.1:p.Asn283=
NM_000507.3:c.849C= NP_000498.2:p.Asn283=
NM_001127628.1:c.849C= NP_001121100.1:p.Asn283=
XM_006717005.2:c.603C= XP_006717068.1:p.Asn201=
XM_006717005.4:c.603C= XP_006717068.1:p.Asn201=
NM_000507.4:c.849C= MANE Select NP_000498.2:p.Asn283=
NM_001127628.2:c.849C= NP_001121100.1:p.Asn283=