Canonical Allele Identifier: CA2579387339

Gene: FBP1

Linked Data

• dbSNP Id: rs2131509076

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639106_94639109dup , CM000671.2:g.94639106_94639109dup	GRCh38
NC_000009.11:g.97401388_97401391dup , CM000671.1:g.97401388_97401391dup	GRCh37
NC_000009.10:g.96441209_96441212dup	NCBI36
NG_008174.1:g.6148_6151dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+39_170+42dup	ENSP00000507547.1:n.170+39_170+42dup
ENST00000375326.9:c.170+39_170+42dup MANE Select	ENSP00000364475.5:n.170+39_170+42dup
ENST00000375326.8:c.170+39_170+42dup	ENSP00000364475.4:n.170+39_170+42dup
ENST00000414122.1:c.-83+942_-83+945dup	ENSP00000411619.1:n.-83+942_-83+945dup
ENST00000415431.5:c.170+39_170+42dup	ENSP00000408025.1:n.170+39_170+42dup
NM_000507.3:c.170+39_170+42dup	NP_000498.2:n.170+39_170+42dup
NM_001127628.1:c.170+39_170+42dup	NP_001121100.1:n.170+39_170+42dup
XM_006717005.2:c.-77+942_-77+945dup	XP_006717068.1:n.-77+942_-77+945dup
XM_006717005.4:c.-77+942_-77+945dup	XP_006717068.1:n.-77+942_-77+945dup
NM_000507.4:c.170+39_170+42dup MANE Select	NP_000498.2:n.170+39_170+42dup
NM_001127628.2:c.170+39_170+42dup	NP_001121100.1:n.170+39_170+42dup