Canonical Allele Identifier: CA374108611

Gene: FBP1

Linked Data

• gnomAD v4: 9-94620396-G-T
• MyVariant Identifiers: chr9:g.97382678G>T (hg19) ; chr9:g.94620396G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94620396G>T , CM000671.2:g.94620396G>T	GRCh38
NC_000009.11:g.97382678G>T , CM000671.1:g.97382678G>T	GRCh37
NC_000009.10:g.96422499G>T	NCBI36
NG_008174.1:g.24854C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.266C>A	ENSP00000507547.1:p.Ser89Tyr
ENST00000375326.9:c.266C>A MANE Select	ENSP00000364475.5:p.Ser89Tyr
ENST00000648117.1:c.164C>A	ENSP00000498145.1:p.Ser55Tyr
ENST00000375326.8:c.266C>A	ENSP00000364475.4:p.Ser89Tyr
ENST00000414122.1:c.14C>A	ENSP00000411619.1:p.Ser5Tyr
ENST00000415431.5:c.266C>A	ENSP00000408025.1:p.Ser89Tyr
NM_000507.3:c.266C>A	NP_000498.2:p.Ser89Tyr
NM_001127628.1:c.266C>A	NP_001121100.1:p.Ser89Tyr
XM_006717005.2:c.20C>A	XP_006717068.1:p.Ser7Tyr
XM_006717005.4:c.20C>A	XP_006717068.1:p.Ser7Tyr
NM_000507.4:c.266C>A MANE Select	NP_000498.2:p.Ser89Tyr
NM_001127628.2:c.266C>A	NP_001121100.1:p.Ser89Tyr