Canonical Allele Identifier: CA367116883

Gene: FKBP14 FKBP14-AS1

Linked Data

• gnomAD v4: 7-30019085-C-A
• MyVariant Identifiers: chr7:g.30058701C>A (hg19) ; chr7:g.30019085C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019085C>A , CM000669.2:g.30019085C>A	GRCh38
NC_000007.13:g.30058701C>A , CM000669.1:g.30058701C>A	GRCh37
NC_000007.12:g.30025226C>A	NCBI36
NG_032173.1:g.12717G>T , LRG_454:g.12717G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.388G>T (FKBP14) MANE Select	ENSP00000222803.5:p.Asp130Tyr
ENST00000222803.9:c.388G>T (FKBP14)	ENSP00000222803.5:p.Asp130Tyr
ENST00000412494.1:c.391G>T (FKBP14)
ENST00000419018.1:c.*35G>T (FKBP14)	ENSP00000406270.1:n.*35G>T
NM_017946.3:c.388G>T , LRG_454t1:c.388G>T (FKBP14)	NP_060416.1:p.Asp130Tyr
NR_046478.1:n.773G>T (FKBP14)
NR_046479.1:n.529G>T (FKBP14)
XR_927144.1:n.1570-6302C>A (FKBP14-AS1)
XR_927145.1:n.1139-6302C>A (FKBP14-AS1)
XR_927145.3:n.345-6302C>A (FKBP14-AS1)
NM_017946.4:c.388G>T (FKBP14) MANE Select	NP_060416.1:p.Asp130Tyr
NR_046478.2:n.674G>T (FKBP14)
NR_046479.2:n.430G>T (FKBP14)