Canonical Allele Identifier: CA156001034
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1044873882
gnomAD v2: 7-30058773-A-G
gnomAD v3: 7-30019157-A-G
gnomAD v4: 7-30019157-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019157A>G , CM000669.2:g.30019157A>G GRCh38
NC_000007.13:g.30058773A>G , CM000669.1:g.30058773A>G GRCh37
NC_000007.12:g.30025298A>G NCBI36
NG_032173.1:g.12645T>C , LRG_454:g.12645T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.350-34T>C (FKBP14) MANE Select ENSP00000222803.5:n.350-34T>C
ENST00000222803.9:c.350-34T>C (FKBP14) ENSP00000222803.5:n.350-34T>C
ENST00000412494.1:c.353-34T>C (FKBP14)
ENST00000419018.1:c.198-34T>C (FKBP14) ENSP00000406270.1:n.198-34T>C
NM_017946.3:c.350-34T>C , LRG_454t1:c.350-34T>C (FKBP14) NP_060416.1:n.350-34T>C
NR_046478.1:n.735-34T>C (FKBP14)
NR_046479.1:n.491-34T>C (FKBP14)
XR_927144.1:n.1570-6230A>G (FKBP14-AS1)
XR_927145.1:n.1139-6230A>G (FKBP14-AS1)
XR_927145.3:n.345-6230A>G (FKBP14-AS1)
NM_017946.4:c.350-34T>C (FKBP14) MANE Select NP_060416.1:n.350-34T>C
NR_046478.2:n.636-34T>C (FKBP14)
NR_046479.2:n.392-34T>C (FKBP14)