Canonical Allele Identifier: CA454237113
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.30058702A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019086A>G , CM000669.2:g.30019086A>G GRCh38
NC_000007.13:g.30058702A>G , CM000669.1:g.30058702A>G GRCh37
NC_000007.12:g.30025227A>G NCBI36
NG_032173.1:g.12716T>C , LRG_454:g.12716T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.387T>C (FKBP14) MANE Select ENSP00000222803.5:p.Ile129=
ENST00000222803.9:c.387T>C (FKBP14) ENSP00000222803.5:p.Ile129=
ENST00000412494.1:c.390T>C (FKBP14)
ENST00000419018.1:c.*34T>C (FKBP14) ENSP00000406270.1:n.*34T>C
NM_017946.3:c.387T>C , LRG_454t1:c.387T>C (FKBP14) NP_060416.1:p.Ile129=
NR_046478.1:n.772T>C (FKBP14)
NR_046479.1:n.528T>C (FKBP14)
XR_927144.1:n.1570-6301A>G (FKBP14-AS1)
XR_927145.1:n.1139-6301A>G (FKBP14-AS1)
XR_927145.3:n.345-6301A>G (FKBP14-AS1)
NM_017946.4:c.387T>C (FKBP14) MANE Select NP_060416.1:p.Ile129=
NR_046478.2:n.673T>C (FKBP14)
NR_046479.2:n.429T>C (FKBP14)