Canonical Allele Identifier: CA1697488953
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019077C= , CM000669.2:g.30019077C= GRCh38
NC_000007.13:g.30058693C= , CM000669.1:g.30058693C= GRCh37
NC_000007.12:g.30025218C= NCBI36
NG_032173.1:g.12725G= , LRG_454:g.12725G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.396G= (FKBP14) MANE Select ENSP00000222803.5:p.Leu132=
ENST00000222803.9:c.396G= (FKBP14) ENSP00000222803.5:p.Leu132=
ENST00000412494.1:c.399G= (FKBP14)
ENST00000419018.1:c.*43G= (FKBP14) ENSP00000406270.1:n.*43G=
NM_017946.3:c.396G= , LRG_454t1:c.396G= (FKBP14) NP_060416.1:p.Leu132=
NR_046478.1:n.781G= (FKBP14)
NR_046479.1:n.537G= (FKBP14)
XR_927144.1:n.1570-6310C= (FKBP14-AS1)
XR_927145.1:n.1139-6310C= (FKBP14-AS1)
XR_927145.3:n.345-6310C= (FKBP14-AS1)
NM_017946.4:c.396G= (FKBP14) MANE Select NP_060416.1:p.Leu132=
NR_046478.2:n.682G= (FKBP14)
NR_046479.2:n.438G= (FKBP14)