Canonical Allele Identifier: CA2260200572
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819482G= , CM000679.2:g.41819482G= GRCh38
NC_000017.10:g.39975734G= , CM000679.1:g.39975734G= GRCh37
NC_000017.9:g.37229260G= NCBI36
NG_015860.1:g.11773G= , LRG_12:g.11773G=

Transcript Alleles

HGVS Amino-acid change
ENST00000706683.1:c.728-787G= ENSP00000516497.1:n.728-787G=
ENST00000321562.9:c.918-48G= MANE Select ENSP00000317232.4:n.918-48G=
ENST00000321562.8:c.918-48G= ENSP00000317232.4:n.918-48G=
ENST00000455106.1:c.146-48G=
ENST00000487489.1:n.531-48G=
ENST00000489591.5:c.*328-48G= ENSP00000466352.1:n.*328-48G=
NM_021939.3:c.918-48G= , LRG_12t1:c.918-48G= NP_068758.3:n.918-48G=
XM_011525099.1:c.918-48G= XP_011523401.1:n.918-48G=
XM_011525100.1:c.645-48G= XP_011523402.1:n.645-48G=
XM_011525099.3:c.918-48G= XP_011523401.1:n.918-48G=
XM_011525100.2:c.645-48G= XP_011523402.1:n.645-48G=
NM_021939.4:c.918-48G= MANE Select NP_068758.3:n.918-48G=