Canonical Allele Identifier: CA2637867328
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819452G>A , CM000679.2:g.41819452G>A GRCh38
NC_000017.10:g.39975704G>A , CM000679.1:g.39975704G>A GRCh37
NC_000017.9:g.37229230G>A NCBI36
NG_015860.1:g.11743G>A , LRG_12:g.11743G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.917+53G>A MANE Select NP_068758.3:n.917+53G>A
ENST00000321562.9:c.917+53G>A MANE Select ENSP00000317232.4:n.917+53G>A
NM_021939.3:c.917+53G>A , LRG_12t1:c.917+53G>A NP_068758.3:n.917+53G>A
ENST00000321562.8:c.917+53G>A ENSP00000317232.4:n.917+53G>A
ENST00000455106.1:c.145+53G>A
ENST00000487489.1:n.530+53G>A
ENST00000489591.5:c.*327+53G>A ENSP00000466352.1:n.*327+53G>A
ENST00000706683.1:c.728-817G>A ENSP00000516497.1:n.728-817G>A
XM_011525099.1:c.917+53G>A XP_011523401.1:n.917+53G>A
XM_011525099.3:c.917+53G>A XP_011523401.1:n.917+53G>A
XM_011525100.1:c.644+53G>A XP_011523402.1:n.644+53G>A
XM_011525100.2:c.644+53G>A XP_011523402.1:n.644+53G>A