Canonical Allele Identifier: CA2260200563
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819469G= , CM000679.2:g.41819469G= GRCh38
NC_000017.10:g.39975721G= , CM000679.1:g.39975721G= GRCh37
NC_000017.9:g.37229247G= NCBI36
NG_015860.1:g.11760G= , LRG_12:g.11760G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706683.1:c.728-800G= ENSP00000516497.1:n.728-800G=
ENST00000321562.9:c.918-61G= MANE Select ENSP00000317232.4:n.918-61G=
ENST00000321562.8:c.918-61G= ENSP00000317232.4:n.918-61G=
ENST00000455106.1:c.146-61G=
ENST00000487489.1:n.531-61G=
ENST00000489591.5:c.*328-61G= ENSP00000466352.1:n.*328-61G=
NM_021939.3:c.918-61G= , LRG_12t1:c.918-61G= NP_068758.3:n.918-61G=
XM_011525099.1:c.918-61G= XP_011523401.1:n.918-61G=
XM_011525100.1:c.645-61G= XP_011523402.1:n.645-61G=
XM_011525099.3:c.918-61G= XP_011523401.1:n.918-61G=
XM_011525100.2:c.645-61G= XP_011523402.1:n.645-61G=
NM_021939.4:c.918-61G= MANE Select NP_068758.3:n.918-61G=