Canonical Allele Identifier: CA2260200574

Gene: FKBP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41819487_41819488delinsGC , CM000679.2:g.41819487_41819488delinsGC	GRCh38
NC_000017.10:g.39975739_39975740delinsGC , CM000679.1:g.39975739_39975740delinsGC	GRCh37
NC_000017.9:g.37229265_37229266delinsGC	NCBI36
NG_015860.1:g.11778_11779delinsGC , LRG_12:g.11778_11779delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706683.1:c.728-782_728-781delinsGC	ENSP00000516497.1:n.728-782_728-781delinsGC
ENST00000321562.9:c.918-43_918-42delinsGC MANE Select	ENSP00000317232.4:n.918-43_918-42delinsGC
ENST00000321562.8:c.918-43_918-42delinsGC	ENSP00000317232.4:n.918-43_918-42delinsGC
ENST00000455106.1:c.146-43_146-42delinsGC
ENST00000487489.1:n.531-43_531-42delinsGC
ENST00000489591.5:c.*328-43_*328-42delinsGC	ENSP00000466352.1:n.*328-43_*328-42delinsGC
NM_021939.3:c.918-43_918-42delinsGC , LRG_12t1:c.918-43_918-42delinsGC	NP_068758.3:n.918-43_918-42delinsGC
XM_011525099.1:c.918-43_918-42delinsGC	XP_011523401.1:n.918-43_918-42delinsGC
XM_011525100.1:c.645-43_645-42delinsGC	XP_011523402.1:n.645-43_645-42delinsGC
XM_011525099.3:c.918-43_918-42delinsGC	XP_011523401.1:n.918-43_918-42delinsGC
XM_011525100.2:c.645-43_645-42delinsGC	XP_011523402.1:n.645-43_645-42delinsGC
NM_021939.4:c.918-43_918-42delinsGC MANE Select	NP_068758.3:n.918-43_918-42delinsGC