Canonical Allele Identifier: CA8566654
Community Standard Title: NM_021939.4(FKBP10):c.1402C>T (p.Arg468Trp)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41821656C>T , CM000679.2:g.41821656C>T GRCh38
NC_000017.10:g.39977908C>T , CM000679.1:g.39977908C>T GRCh37
NC_000017.9:g.37231434C>T NCBI36
NG_015860.1:g.13947C>T , LRG_12:g.13947C>T

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.1402C>T MANE Select NP_068758.3:p.Arg468Trp
ENST00000321562.9:c.1402C>T MANE Select ENSP00000317232.4:p.Arg468Trp
NM_021939.3:c.1402C>T , LRG_12t1:c.1402C>T NP_068758.3:p.Arg468Trp
ENST00000321562.8:c.1402C>T ENSP00000317232.4:p.Arg468Trp
ENST00000455106.1:c.813C>T
ENST00000464180.1:n.650C>T
ENST00000489591.5:c.*1186C>T ENSP00000466352.1:n.*1186C>T
ENST00000490938.5:n.605C>T
ENST00000706683.1:c.1066C>T ENSP00000516497.1:p.Arg356Trp
XM_011525099.1:c.1459C>T XP_011523401.1:p.Arg487Trp
XM_011525099.3:c.1459C>T XP_011523401.1:p.Arg487Trp
XM_011525100.1:c.1186C>T XP_011523402.1:p.Arg396Trp
XM_011525100.2:c.1186C>T XP_011523402.1:p.Arg396Trp