Canonical Allele Identifier: CA454237091
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.30058675T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019059T>A , CM000669.2:g.30019059T>A GRCh38
NC_000007.13:g.30058675T>A , CM000669.1:g.30058675T>A GRCh37
NC_000007.12:g.30025200T>A NCBI36
NG_032173.1:g.12743A>T , LRG_454:g.12743A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.414A>T (FKBP14) MANE Select ENSP00000222803.5:p.Pro138=
ENST00000222803.9:c.414A>T (FKBP14) ENSP00000222803.5:p.Pro138=
ENST00000412494.1:c.417A>T (FKBP14)
ENST00000419018.1:c.*61A>T (FKBP14) ENSP00000406270.1:n.*61A>T
NM_017946.3:c.414A>T , LRG_454t1:c.414A>T (FKBP14) NP_060416.1:p.Pro138=
NR_046478.1:n.799A>T (FKBP14)
NR_046479.1:n.555A>T (FKBP14)
XR_927144.1:n.1570-6328T>A (FKBP14-AS1)
XR_927145.1:n.1139-6328T>A (FKBP14-AS1)
XR_927145.3:n.345-6328T>A (FKBP14-AS1)
NM_017946.4:c.414A>T (FKBP14) MANE Select NP_060416.1:p.Pro138=
NR_046478.2:n.700A>T (FKBP14)
NR_046479.2:n.456A>T (FKBP14)