Canonical Allele Identifier: CA374106704

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97369134G>A (hg19) ; chr9:g.94606852G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94606852G>A , CM000671.2:g.94606852G>A	GRCh38
NC_000009.11:g.97369134G>A , CM000671.1:g.97369134G>A	GRCh37
NC_000009.10:g.96408955G>A	NCBI36
NG_008174.1:g.38398C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.828C>T	ENSP00000507547.1:n.828C>T
ENST00000375326.9:c.668C>T MANE Select	ENSP00000364475.5:p.Ala223Val
ENST00000648117.1:c.473C>T	ENSP00000498145.1:p.Ala158Val
ENST00000375326.8:c.668C>T	ENSP00000364475.4:p.Ala223Val
ENST00000414122.1:c.416C>T	ENSP00000411619.1:p.Ala139Val
ENST00000415431.5:c.668C>T	ENSP00000408025.1:p.Ala223Val
NM_000507.3:c.668C>T	NP_000498.2:p.Ala223Val
NM_001127628.1:c.668C>T	NP_001121100.1:p.Ala223Val
XM_006717005.2:c.422C>T	XP_006717068.1:p.Ala141Val
XM_006717005.4:c.422C>T	XP_006717068.1:p.Ala141Val
NM_000507.4:c.668C>T MANE Select	NP_000498.2:p.Ala223Val
NM_001127628.2:c.668C>T	NP_001121100.1:p.Ala223Val