Canonical Allele Identifier: CA399513479

Gene: FKBP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41813140C>A , CM000679.2:g.41813140C>A	GRCh38
NC_000017.10:g.39969392C>A , CM000679.1:g.39969392C>A	GRCh37
NC_000017.9:g.37222918C>A	NCBI36
NG_015860.1:g.5431C>A , LRG_12:g.5431C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021939.4:c.106C>A MANE Select	NP_068758.3:p.Pro36Thr
ENST00000321562.9:c.106C>A MANE Select	ENSP00000317232.4:p.Pro36Thr
NM_021939.3:c.106C>A , LRG_12t1:c.106C>A	NP_068758.3:p.Pro36Thr
ENST00000321562.8:c.106C>A	ENSP00000317232.4:p.Pro36Thr
ENST00000429461.5:c.-22-53C>A	ENSP00000408232.1:n.-22-53C>A
ENST00000489591.5:c.106C>A	ENSP00000466352.1:p.Pro36Thr
ENST00000585664.5:c.-22-53C>A	ENSP00000468703.1:n.-22-53C>A
ENST00000585922.5:c.106C>A	ENSP00000466097.1:p.Pro36Thr
ENST00000706683.1:c.106C>A	ENSP00000516497.1:p.Pro36Thr
XM_011525099.1:c.106C>A	XP_011523401.1:p.Pro36Thr
XM_011525099.3:c.106C>A	XP_011523401.1:p.Pro36Thr
XM_011525100.1:c.-22C>A	XP_011523402.1:n.-22C>A
XM_011525100.2:c.-22C>A	XP_011523402.1:n.-22C>A