Canonical Allele Identifier: CA1697489120
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019150T= , CM000669.2:g.30019150T= GRCh38
NC_000007.13:g.30058766T= , CM000669.1:g.30058766T= GRCh37
NC_000007.12:g.30025291T= NCBI36
NG_032173.1:g.12652A= , LRG_454:g.12652A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.350-27A= (FKBP14) MANE Select ENSP00000222803.5:n.350-27A=
ENST00000222803.9:c.350-27A= (FKBP14) ENSP00000222803.5:n.350-27A=
ENST00000412494.1:c.353-27A= (FKBP14)
ENST00000419018.1:c.198-27A= (FKBP14) ENSP00000406270.1:n.198-27A=
NM_017946.3:c.350-27A= , LRG_454t1:c.350-27A= (FKBP14) NP_060416.1:n.350-27A=
NR_046478.1:n.735-27A= (FKBP14)
NR_046479.1:n.491-27A= (FKBP14)
XR_927144.1:n.1570-6237T= (FKBP14-AS1)
XR_927145.1:n.1139-6237T= (FKBP14-AS1)
XR_927145.3:n.345-6237T= (FKBP14-AS1)
NM_017946.4:c.350-27A= (FKBP14) MANE Select NP_060416.1:n.350-27A=
NR_046478.2:n.636-27A= (FKBP14)
NR_046479.2:n.392-27A= (FKBP14)