Canonical Allele Identifier: CA2260200564
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819473C= , CM000679.2:g.41819473C= GRCh38
NC_000017.10:g.39975725C= , CM000679.1:g.39975725C= GRCh37
NC_000017.9:g.37229251C= NCBI36
NG_015860.1:g.11764C= , LRG_12:g.11764C=

Transcript Alleles

HGVS Amino-acid change
ENST00000706683.1:c.728-796C= ENSP00000516497.1:n.728-796C=
ENST00000321562.9:c.918-57C= MANE Select ENSP00000317232.4:n.918-57C=
ENST00000321562.8:c.918-57C= ENSP00000317232.4:n.918-57C=
ENST00000455106.1:c.146-57C=
ENST00000487489.1:n.531-57C=
ENST00000489591.5:c.*328-57C= ENSP00000466352.1:n.*328-57C=
NM_021939.3:c.918-57C= , LRG_12t1:c.918-57C= NP_068758.3:n.918-57C=
XM_011525099.1:c.918-57C= XP_011523401.1:n.918-57C=
XM_011525100.1:c.645-57C= XP_011523402.1:n.645-57C=
XM_011525099.3:c.918-57C= XP_011523401.1:n.918-57C=
XM_011525100.2:c.645-57C= XP_011523402.1:n.645-57C=
NM_021939.4:c.918-57C= MANE Select NP_068758.3:n.918-57C=