Canonical Allele Identifier: CA8566387
Community Standard Title: NM_021939.4(FKBP10):c.850G>A (p.Gly284Arg)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819332G>A , CM000679.2:g.41819332G>A GRCh38
NC_000017.10:g.39975584G>A , CM000679.1:g.39975584G>A GRCh37
NC_000017.9:g.37229110G>A NCBI36
NG_015860.1:g.11623G>A , LRG_12:g.11623G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.850G>A MANE Select NP_068758.3:p.Gly284Arg
ENST00000321562.9:c.850G>A MANE Select ENSP00000317232.4:p.Gly284Arg
NM_021939.3:c.850G>A , LRG_12t1:c.850G>A NP_068758.3:p.Gly284Arg
ENST00000321562.8:c.850G>A ENSP00000317232.4:p.Gly284Arg
ENST00000455106.1:c.78G>A
ENST00000487489.1:n.463G>A
ENST00000489591.5:c.*260G>A ENSP00000466352.1:n.*260G>A
ENST00000706683.1:c.727+805G>A ENSP00000516497.1:n.727+805G>A
XM_011525099.1:c.850G>A XP_011523401.1:p.Gly284Arg
XM_011525099.3:c.850G>A XP_011523401.1:p.Gly284Arg
XM_011525100.1:c.577G>A XP_011523402.1:p.Gly193Arg
XM_011525100.2:c.577G>A XP_011523402.1:p.Gly193Arg