Canonical Allele Identifier: CA2260200463
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819564G= , CM000679.2:g.41819564G= GRCh38
NC_000017.10:g.39975816G= , CM000679.1:g.39975816G= GRCh37
NC_000017.9:g.37229342G= NCBI36
NG_015860.1:g.11855G= , LRG_12:g.11855G=

Transcript Alleles

HGVS Amino-acid change
ENST00000706683.1:c.728-705G= ENSP00000516497.1:n.728-705G=
ENST00000321562.9:c.952G= MANE Select ENSP00000317232.4:p.Gly318=
ENST00000321562.8:c.952G= ENSP00000317232.4:p.Gly318=
ENST00000455106.1:c.180G=
ENST00000487489.1:n.565G=
ENST00000489591.5:c.*362G= ENSP00000466352.1:n.*362G=
NM_021939.3:c.952G= , LRG_12t1:c.952G= NP_068758.3:p.Gly318=
XM_011525099.1:c.952G= XP_011523401.1:p.Gly318=
XM_011525100.1:c.679G= XP_011523402.1:p.Gly227=
XM_011525099.3:c.952G= XP_011523401.1:p.Gly318=
XM_011525100.2:c.679G= XP_011523402.1:p.Gly227=
NM_021939.4:c.952G= MANE Select NP_068758.3:p.Gly318=