Canonical Allele Identifier: CA1865226061

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605552_94605562delinsGGGCCCCATAA , CM000671.2:g.94605552_94605562delinsGGGCCCCATAA	GRCh38
NC_000009.11:g.97367834_97367844delinsGGGCCCCATAA , CM000671.1:g.97367834_97367844delinsGGGCCCCATAA	GRCh37
NC_000009.10:g.96407655_96407665delinsGGGCCCCATAA	NCBI36
NG_008174.1:g.39688_39698delinsTTATGGGGCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.880_890delinsTTATGGGGCCC	ENSP00000507547.1:n.880_890delinsTTATGGGG...
ENST00000375326.9:c.720_730delinsTTATGGGGCCC MANE Select	ENSP00000364475.5:p.Pro240=
ENST00000648117.1:c.525_535delinsTTATGGGGCCC	ENSP00000498145.1:p.Pro175=
ENST00000375326.8:c.720_730delinsTTATGGGGCCC	ENSP00000364475.4:p.Pro240=
ENST00000415431.5:c.720_730delinsTTATGGGGCCC	ENSP00000408025.1:p.Pro240=
NM_000507.3:c.720_730delinsTTATGGGGCCC	NP_000498.2:p.Pro240=
NM_001127628.1:c.720_730delinsTTATGGGGCCC	NP_001121100.1:p.Pro240=
XM_006717005.2:c.474_484delinsTTATGGGGCCC	XP_006717068.1:p.Pro158=
XM_006717005.4:c.474_484delinsTTATGGGGCCC	XP_006717068.1:p.Pro158=
NM_000507.4:c.720_730delinsTTATGGGGCCC MANE Select	NP_000498.2:p.Pro240=
NM_001127628.2:c.720_730delinsTTATGGGGCCC	NP_001121100.1:p.Pro240=