Canonical Allele Identifier: CA374107609

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97372208C>A (hg19) ; chr9:g.94609926C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94609926C>A , CM000671.2:g.94609926C>A	GRCh38
NC_000009.11:g.97372208C>A , CM000671.1:g.97372208C>A	GRCh37
NC_000009.10:g.96412029C>A	NCBI36
NG_008174.1:g.35324G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.562G>T	ENSP00000507547.1:p.Asp188Tyr
ENST00000375326.9:c.562G>T MANE Select	ENSP00000364475.5:p.Asp188Tyr
ENST00000648117.1:c.367G>T	ENSP00000498145.1:p.Asp123Tyr
ENST00000375326.8:c.562G>T	ENSP00000364475.4:p.Asp188Tyr
ENST00000414122.1:c.310G>T	ENSP00000411619.1:p.Asp104Tyr
ENST00000415431.5:c.562G>T	ENSP00000408025.1:p.Asp188Tyr
NM_000507.3:c.562G>T	NP_000498.2:p.Asp188Tyr
NM_001127628.1:c.562G>T	NP_001121100.1:p.Asp188Tyr
XM_006717005.2:c.316G>T	XP_006717068.1:p.Asp106Tyr
XM_006717005.4:c.316G>T	XP_006717068.1:p.Asp106Tyr
NM_000507.4:c.562G>T MANE Select	NP_000498.2:p.Asp188Tyr
NM_001127628.2:c.562G>T	NP_001121100.1:p.Asp188Tyr