Canonical Allele Identifier: CA454237105
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.30058693C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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