Canonical Allele Identifier: CA374106332

Gene: FBP1

Linked Data

• COSMIC: COSM4509687
• MyVariant Identifiers: chr9:g.97367750G>A (hg19) ; chr9:g.94605468G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605468G>A , CM000671.2:g.94605468G>A	GRCh38
NC_000009.11:g.97367750G>A , CM000671.1:g.97367750G>A	GRCh37
NC_000009.10:g.96407571G>A	NCBI36
NG_008174.1:g.39782C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.974C>T	ENSP00000507547.1:n.974C>T
ENST00000375326.9:c.814C>T MANE Select	ENSP00000364475.5:p.Pro272Ser
ENST00000648117.1:c.619C>T	ENSP00000498145.1:p.Pro207Ser
ENST00000375326.8:c.814C>T	ENSP00000364475.4:p.Pro272Ser
ENST00000415431.5:c.814C>T	ENSP00000408025.1:p.Pro272Ser
NM_000507.3:c.814C>T	NP_000498.2:p.Pro272Ser
NM_001127628.1:c.814C>T	NP_001121100.1:p.Pro272Ser
XM_006717005.2:c.568C>T	XP_006717068.1:p.Pro190Ser
XM_006717005.4:c.568C>T	XP_006717068.1:p.Pro190Ser
NM_000507.4:c.814C>T MANE Select	NP_000498.2:p.Pro272Ser
NM_001127628.2:c.814C>T	NP_001121100.1:p.Pro272Ser