Canonical Allele Identifier: CA1865225181
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94603547G= , CM000671.2:g.94603547G= GRCh38
NC_000009.11:g.97365829G= , CM000671.1:g.97365829G= GRCh37
NC_000009.10:g.96405650G= NCBI36
NG_008174.1:g.41703C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.1011C= ENSP00000507547.1:n.1011C=
ENST00000375326.9:c.851C= MANE Select ENSP00000364475.5:p.Pro284=
ENST00000648117.1:c.656C= ENSP00000498145.1:p.Pro219=
ENST00000375326.8:c.851C= ENSP00000364475.4:p.Pro284=
ENST00000415431.5:c.851C= ENSP00000408025.1:p.Pro284=
NM_000507.3:c.851C= NP_000498.2:p.Pro284=
NM_001127628.1:c.851C= NP_001121100.1:p.Pro284=
XM_006717005.2:c.605C= XP_006717068.1:p.Pro202=
XM_006717005.4:c.605C= XP_006717068.1:p.Pro202=
NM_000507.4:c.851C= MANE Select NP_000498.2:p.Pro284=
NM_001127628.2:c.851C= NP_001121100.1:p.Pro284=