Canonical Allele Identifier: CA454237099
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.30058684T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019068T>C , CM000669.2:g.30019068T>C GRCh38
NC_000007.13:g.30058684T>C , CM000669.1:g.30058684T>C GRCh37
NC_000007.12:g.30025209T>C NCBI36
NG_032173.1:g.12734A>G , LRG_454:g.12734A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.405A>G (FKBP14) MANE Select ENSP00000222803.5:p.Arg135=
ENST00000222803.9:c.405A>G (FKBP14) ENSP00000222803.5:p.Arg135=
ENST00000412494.1:c.408A>G (FKBP14)
ENST00000419018.1:c.*52A>G (FKBP14) ENSP00000406270.1:n.*52A>G
NM_017946.3:c.405A>G , LRG_454t1:c.405A>G (FKBP14) NP_060416.1:p.Arg135=
NR_046478.1:n.790A>G (FKBP14)
NR_046479.1:n.546A>G (FKBP14)
XR_927144.1:n.1570-6319T>C (FKBP14-AS1)
XR_927145.1:n.1139-6319T>C (FKBP14-AS1)
XR_927145.3:n.345-6319T>C (FKBP14-AS1)
NM_017946.4:c.405A>G (FKBP14) MANE Select NP_060416.1:p.Arg135=
NR_046478.2:n.691A>G (FKBP14)
NR_046479.2:n.447A>G (FKBP14)