Canonical Allele Identifier: CA8566564

Gene: FKBP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41820472G>T , CM000679.2:g.41820472G>T	GRCh38
NC_000017.10:g.39976724G>T , CM000679.1:g.39976724G>T	GRCh37
NC_000017.9:g.37230250G>T	NCBI36
NG_015860.1:g.12763G>T , LRG_12:g.12763G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021939.4:c.1256+11G>T MANE Select	NP_068758.3:n.1256+11G>T
ENST00000321562.9:c.1256+11G>T MANE Select	ENSP00000317232.4:n.1256+11G>T
NM_021939.3:c.1256+11G>T , LRG_12t1:c.1256+11G>T	NP_068758.3:n.1256+11G>T
ENST00000321562.8:c.1256+11G>T	ENSP00000317232.4:n.1256+11G>T
ENST00000455106.1:c.667+11G>T
ENST00000464180.1:n.30G>T
ENST00000489591.5:c.*1040+11G>T	ENSP00000466352.1:n.*1040+11G>T
ENST00000490938.5:n.459+11G>T
ENST00000706683.1:c.920+11G>T	ENSP00000516497.1:n.920+11G>T
XM_011525099.1:c.1256+11G>T	XP_011523401.1:n.1256+11G>T
XM_011525099.3:c.1256+11G>T	XP_011523401.1:n.1256+11G>T
XM_011525100.1:c.983+11G>T	XP_011523402.1:n.983+11G>T
XM_011525100.2:c.983+11G>T	XP_011523402.1:n.983+11G>T