Canonical Allele Identifier: CA399518986

Gene: FKBP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41821818G>A , CM000679.2:g.41821818G>A	GRCh38
NC_000017.10:g.39978070G>A , CM000679.1:g.39978070G>A	GRCh37
NC_000017.9:g.37231596G>A	NCBI36
NG_015860.1:g.14109G>A , LRG_12:g.14109G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021939.4:c.1563+1G>A MANE Select	NP_068758.3:n.1563+1G>A
ENST00000321562.9:c.1563+1G>A MANE Select	ENSP00000317232.4:n.1563+1G>A
NM_021939.3:c.1563+1G>A , LRG_12t1:c.1563+1G>A	NP_068758.3:n.1563+1G>A
ENST00000321562.8:c.1563+1G>A	ENSP00000317232.4:n.1563+1G>A
ENST00000455106.1:c.974+1G>A
ENST00000464180.1:n.811+1G>A
ENST00000489591.5:c.*1347+1G>A	ENSP00000466352.1:n.*1347+1G>A
ENST00000490938.5:n.766+1G>A
ENST00000706683.1:c.1227+1G>A	ENSP00000516497.1:n.1227+1G>A
XM_011525099.1:c.1620+1G>A	XP_011523401.1:n.1620+1G>A
XM_011525099.3:c.1620+1G>A	XP_011523401.1:n.1620+1G>A
XM_011525100.1:c.1347+1G>A	XP_011523402.1:n.1347+1G>A
XM_011525100.2:c.1347+1G>A	XP_011523402.1:n.1347+1G>A