Canonical Allele Identifier: CA399516497
Community Standard Title: NM_021939.4(FKBP10):c.850G>C (p.Gly284Arg)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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