Canonical Allele Identifier: CA8566615
Community Standard Title: NM_021939.4(FKBP10):c.1323G>A (p.Thr441=)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41821013G>A , CM000679.2:g.41821013G>A GRCh38
NC_000017.10:g.39977265G>A , CM000679.1:g.39977265G>A GRCh37
NC_000017.9:g.37230791G>A NCBI36
NG_015860.1:g.13304G>A , LRG_12:g.13304G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.1323G>A MANE Select NP_068758.3:p.Thr441=
ENST00000321562.9:c.1323G>A MANE Select ENSP00000317232.4:p.Thr441=
NM_021939.3:c.1323G>A , LRG_12t1:c.1323G>A NP_068758.3:p.Thr441=
ENST00000321562.8:c.1323G>A ENSP00000317232.4:p.Thr441=
ENST00000455106.1:c.734G>A
ENST00000464180.1:n.571G>A
ENST00000489591.5:c.*1107G>A ENSP00000466352.1:n.*1107G>A
ENST00000490938.5:n.526G>A
ENST00000706683.1:c.987G>A ENSP00000516497.1:p.Thr329=
XM_011525099.1:c.1380G>A XP_011523401.1:p.Thr460=
XM_011525099.3:c.1380G>A XP_011523401.1:p.Thr460=
XM_011525100.1:c.1107G>A XP_011523402.1:p.Thr369=
XM_011525100.2:c.1107G>A XP_011523402.1:p.Thr369=