Canonical Allele Identifier: CA2564383774

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94638852_94638853insTTTCTAATCCAGTTAT , CM000671.2:g.94638852_94638853insTTTCTAATCCAGTTAT	GRCh38
NC_000009.11:g.97401134_97401135insTTTCTAATCCAGTTAT , CM000671.1:g.97401134_97401135insTTTCTAATCCAGTTAT	GRCh37
NC_000009.10:g.96440955_96440956insTTTCTAATCCAGTTAT	NCBI36
NG_008174.1:g.6397_6398insATAACTGGATTAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+288_170+289insATAACTGGATTAGAAA	ENSP00000507547.1:n.170+288_170+289insATAACTGGATTAGAAA
ENST00000375326.9:c.170+288_170+289insATAACTGGATTAGAAA MANE Select	ENSP00000364475.5:n.170+288_170+289insATAACTGGATTAGAAA
ENST00000375326.8:c.170+288_170+289insATAACTGGATTAGAAA	ENSP00000364475.4:n.170+288_170+289insATAACTGGATTAGAAA
ENST00000414122.1:c.-83+1191_-83+1192insATAACTGGATTAGAAA	ENSP00000411619.1:n.-83+1191_-83+1192insATAACTGGATTAGAAA
ENST00000415431.5:c.170+288_170+289insATAACTGGATTAGAAA	ENSP00000408025.1:n.170+288_170+289insATAACTGGATTAGAAA
NM_000507.3:c.170+288_170+289insATAACTGGATTAGAAA	NP_000498.2:n.170+288_170+289insATAACTGGATTAGAAA
NM_001127628.1:c.170+288_170+289insATAACTGGATTAGAAA	NP_001121100.1:n.170+288_170+289insATAACTGGATTAGAAA
XM_006717005.2:c.-77+1191_-77+1192insATAACTGGATTAGAAA	XP_006717068.1:n.-77+1191_-77+1192insATAACTGGATTAGAAA
XM_006717005.4:c.-77+1191_-77+1192insATAACTGGATTAGAAA	XP_006717068.1:n.-77+1191_-77+1192insATAACTGGATTAGAAA
NM_000507.4:c.170+288_170+289insATAACTGGATTAGAAA MANE Select	NP_000498.2:n.170+288_170+289insATAACTGGATTAGAAA
NM_001127628.2:c.170+288_170+289insATAACTGGATTAGAAA	NP_001121100.1:n.170+288_170+289insATAACTGGATTAGAAA