Canonical Allele Identifier: CA466102924

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97382683C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94620401C>T , CM000671.2:g.94620401C>T	GRCh38
NC_000009.11:g.97382683C>T , CM000671.1:g.97382683C>T	GRCh37
NC_000009.10:g.96422504C>T	NCBI36
NG_008174.1:g.24849G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.261G>A	ENSP00000507547.1:p.Lys87=
ENST00000375326.9:c.261G>A MANE Select	ENSP00000364475.5:p.Lys87=
ENST00000648117.1:c.159G>A	ENSP00000498145.1:p.Lys53=
ENST00000375326.8:c.261G>A	ENSP00000364475.4:p.Lys87=
ENST00000414122.1:c.9G>A	ENSP00000411619.1:p.Lys3=
ENST00000415431.5:c.261G>A	ENSP00000408025.1:p.Lys87=
NM_000507.3:c.261G>A	NP_000498.2:p.Lys87=
NM_001127628.1:c.261G>A	NP_001121100.1:p.Lys87=
XM_006717005.2:c.15G>A	XP_006717068.1:p.Lys5=
XM_006717005.4:c.15G>A	XP_006717068.1:p.Lys5=
NM_000507.4:c.261G>A MANE Select	NP_000498.2:p.Lys87=
NM_001127628.2:c.261G>A	NP_001121100.1:p.Lys87=