Canonical Allele Identifier: CA1865240159
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94620507G= , CM000671.2:g.94620507G= GRCh38
NC_000009.11:g.97382789G= , CM000671.1:g.97382789G= GRCh37
NC_000009.10:g.96422610G= NCBI36
NG_008174.1:g.24743C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.171-16C= ENSP00000507547.1:n.171-16C=
ENST00000375326.9:c.171-16C= MANE Select ENSP00000364475.5:n.171-16C=
ENST00000648117.1:c.69-16C= ENSP00000498145.1:n.69-16C=
ENST00000375326.8:c.171-16C= ENSP00000364475.4:n.171-16C=
ENST00000414122.1:c.-82-16C= ENSP00000411619.1:n.-82-16C=
ENST00000415431.5:c.171-16C= ENSP00000408025.1:n.171-16C=
NM_000507.3:c.171-16C= NP_000498.2:n.171-16C=
NM_001127628.1:c.171-16C= NP_001121100.1:n.171-16C=
XM_006717005.2:c.-76-16C= XP_006717068.1:n.-76-16C=
XM_006717005.4:c.-76-16C= XP_006717068.1:n.-76-16C=
NM_000507.4:c.171-16C= MANE Select NP_000498.2:n.171-16C=
NM_001127628.2:c.171-16C= NP_001121100.1:n.171-16C=