Canonical Allele Identifier: CA196553557
Gene: FBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94606867_94606869delinsTTA , CM000671.2:g.94606867_94606869delinsTTA GRCh38
NC_000009.11:g.97369149_97369151delinsTTA , CM000671.1:g.97369149_97369151delinsTTA GRCh37
NC_000009.10:g.96408970_96408972delinsTTA NCBI36
NG_008174.1:g.38381_38383delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000682520.1:c.811_813delinsTAA ENSP00000507547.1:n.811_813delinsTAA
ENST00000375326.9:c.651_653delinsTAA MANE Select ENSP00000364475.5:p.Arg218Lys
ENST00000648117.1:c.456_458delinsTAA ENSP00000498145.1:p.Arg153Lys
ENST00000375326.8:c.651_653delinsTAA ENSP00000364475.4:p.Arg218Lys
ENST00000414122.1:c.399_401delinsTAA ENSP00000411619.1:p.Arg134Lys
ENST00000415431.5:c.651_653delinsTAA ENSP00000408025.1:p.Arg218Lys
NM_000507.3:c.651_653delinsTAA NP_000498.2:p.Arg218Lys
NM_001127628.1:c.651_653delinsTAA NP_001121100.1:p.Arg218Lys
XM_006717005.2:c.405_407delinsTAA XP_006717068.1:p.Arg136Lys
XM_006717005.4:c.405_407delinsTAA XP_006717068.1:p.Arg136Lys
NM_000507.4:c.651_653delinsTAA MANE Select NP_000498.2:p.Arg218Lys
NM_001127628.2:c.651_653delinsTAA NP_001121100.1:p.Arg218Lys