Canonical Allele Identifier: CA8566563

Gene: FKBP10

Genomic Alleles

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

Transcript Alleles

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