Canonical Allele Identifier: CA1697488862
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019031C= , CM000669.2:g.30019031C= GRCh38
NC_000007.13:g.30058647C= , CM000669.1:g.30058647C= GRCh37
NC_000007.12:g.30025172C= NCBI36
NG_032173.1:g.12771G= , LRG_454:g.12771G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.442G= (FKBP14) MANE Select ENSP00000222803.5:p.Asp148=
ENST00000222803.9:c.442G= (FKBP14) ENSP00000222803.5:p.Asp148=
ENST00000412494.1:c.445G= (FKBP14)
ENST00000419018.1:c.*89G= (FKBP14) ENSP00000406270.1:n.*89G=
NM_017946.3:c.442G= , LRG_454t1:c.442G= (FKBP14) NP_060416.1:p.Asp148=
NR_046478.1:n.827G= (FKBP14)
NR_046479.1:n.583G= (FKBP14)
XR_927144.1:n.1570-6356C= (FKBP14-AS1)
XR_927145.1:n.1139-6356C= (FKBP14-AS1)
XR_927145.3:n.345-6356C= (FKBP14-AS1)
NM_017946.4:c.442G= (FKBP14) MANE Select NP_060416.1:p.Asp148=
NR_046478.2:n.728G= (FKBP14)
NR_046479.2:n.484G= (FKBP14)