Canonical Allele Identifier: CA381341605

Gene: FIBP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65887955C>T , CM000673.2:g.65887955C>T	GRCh38
NC_000011.9:g.65655426C>T , CM000673.1:g.65655426C>T	GRCh37
NC_000011.8:g.65412002C>T	NCBI36
NG_047103.1:g.5585G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004214.5:c.263G>A MANE Select	NP_004205.2:p.Arg88Gln
ENST00000357519.9:c.263G>A MANE Select	ENSP00000350124.5:p.Arg88Gln
NM_004214.4:c.263G>A	NP_004205.2:p.Arg88Gln
NM_198897.1:c.263G>A	NP_942600.1:p.Arg88Gln
NM_198897.2:c.263G>A	NP_942600.1:p.Arg88Gln
ENST00000338369.6:c.263G>A	ENSP00000344572.2:p.Arg88Gln
ENST00000357519.8:c.263G>A	ENSP00000350124.4:p.Arg88Gln
ENST00000426652.6:n.306G>A
ENST00000442885.2:n.355G>A
ENST00000528937.1:n.358G>A
ENST00000532229.1:c.263G>A	ENSP00000433683.1:p.Arg88Gln
ENST00000532679.5:n.306G>A
ENST00000533037.5:c.263G>A	ENSP00000431414.1:p.Arg88Gln
ENST00000533045.5:c.254G>A	ENSP00000434043.1:p.Arg85Gln
XM_024448763.1:c.-195G>A	XP_024304531.1:n.-195G>A
XR_001748030.2:n.355G>A
XR_950100.1:n.358G>A
XR_950100.2:n.355G>A