Canonical Allele Identifier: CA1697488872
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019032C= , CM000669.2:g.30019032C= GRCh38
NC_000007.13:g.30058648C= , CM000669.1:g.30058648C= GRCh37
NC_000007.12:g.30025173C= NCBI36
NG_032173.1:g.12770G= , LRG_454:g.12770G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.441G= (FKBP14) MANE Select ENSP00000222803.5:p.Met147=
ENST00000222803.9:c.441G= (FKBP14) ENSP00000222803.5:p.Met147=
ENST00000412494.1:c.444G= (FKBP14)
ENST00000419018.1:c.*88G= (FKBP14) ENSP00000406270.1:n.*88G=
NM_017946.3:c.441G= , LRG_454t1:c.441G= (FKBP14) NP_060416.1:p.Met147=
NR_046478.1:n.826G= (FKBP14)
NR_046479.1:n.582G= (FKBP14)
XR_927144.1:n.1570-6355C= (FKBP14-AS1)
XR_927145.1:n.1139-6355C= (FKBP14-AS1)
XR_927145.3:n.345-6355C= (FKBP14-AS1)
NM_017946.4:c.441G= (FKBP14) MANE Select NP_060416.1:p.Met147=
NR_046478.2:n.727G= (FKBP14)
NR_046479.2:n.483G= (FKBP14)