Canonical Allele Identifier: CA1865264686

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94638794_94638807delinsGGGTATGACGGGCA , CM000671.2:g.94638794_94638807delinsGGGTATGACGGGCA	GRCh38
NC_000009.11:g.97401076_97401089delinsGGGTATGACGGGCA , CM000671.1:g.97401076_97401089delinsGGGTATGACGGGCA	GRCh37
NC_000009.10:g.96440897_96440910delinsGGGTATGACGGGCA	NCBI36
NG_008174.1:g.6443_6456delinsTGCCCGTCATACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+334_170+347delinsTGCCCGTCATACCC	ENSP00000507547.1:n.170+334_170+347delinsTGCCCGTCATACCC
ENST00000375326.9:c.170+334_170+347delinsTGCCCGTCATACCC MANE Select	ENSP00000364475.5:n.170+334_170+347delinsTGCCCGTCATACCC
ENST00000375326.8:c.170+334_170+347delinsTGCCCGTCATACCC	ENSP00000364475.4:n.170+334_170+347delinsTGCCCGTCATACCC
ENST00000414122.1:c.-83+1237_-83+1250delinsTGCCCGTCATACCC	ENSP00000411619.1:n.-83+1237_-83+1250delinsTGCCCGTCATACCC
ENST00000415431.5:c.170+334_170+347delinsTGCCCGTCATACCC	ENSP00000408025.1:n.170+334_170+347delinsTGCCCGTCATACCC
NM_000507.3:c.170+334_170+347delinsTGCCCGTCATACCC	NP_000498.2:n.170+334_170+347delinsTGCCCGTCATACCC
NM_001127628.1:c.170+334_170+347delinsTGCCCGTCATACCC	NP_001121100.1:n.170+334_170+347delinsTGCCCGTCATACCC
XM_006717005.2:c.-77+1237_-77+1250delinsTGCCCGTCATACCC	XP_006717068.1:n.-77+1237_-77+1250delinsTGCCCGTCATACCC
XM_006717005.4:c.-77+1237_-77+1250delinsTGCCCGTCATACCC	XP_006717068.1:n.-77+1237_-77+1250delinsTGCCCGTCATACCC
NM_000507.4:c.170+334_170+347delinsTGCCCGTCATACCC MANE Select	NP_000498.2:n.170+334_170+347delinsTGCCCGTCATACCC
NM_001127628.2:c.170+334_170+347delinsTGCCCGTCATACCC	NP_001121100.1:n.170+334_170+347delinsTGCCCGTCATACCC