Canonical Allele Identifier: CA367116879

Gene: FKBP14 FKBP14-AS1

Linked Data

• MyVariant Identifiers: chr7:g.30058699A>T (hg19) ; chr7:g.30019083A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019083A>T , CM000669.2:g.30019083A>T	GRCh38
NC_000007.13:g.30058699A>T , CM000669.1:g.30058699A>T	GRCh37
NC_000007.12:g.30025224A>T	NCBI36
NG_032173.1:g.12719T>A , LRG_454:g.12719T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.390T>A (FKBP14) MANE Select	ENSP00000222803.5:p.Asp130Glu
ENST00000222803.9:c.390T>A (FKBP14)	ENSP00000222803.5:p.Asp130Glu
ENST00000412494.1:c.393T>A (FKBP14)
ENST00000419018.1:c.*37T>A (FKBP14)	ENSP00000406270.1:n.*37T>A
NM_017946.3:c.390T>A , LRG_454t1:c.390T>A (FKBP14)	NP_060416.1:p.Asp130Glu
NR_046478.1:n.775T>A (FKBP14)
NR_046479.1:n.531T>A (FKBP14)
XR_927144.1:n.1570-6304A>T (FKBP14-AS1)
XR_927145.1:n.1139-6304A>T (FKBP14-AS1)
XR_927145.3:n.345-6304A>T (FKBP14-AS1)
NM_017946.4:c.390T>A (FKBP14) MANE Select	NP_060416.1:p.Asp130Glu
NR_046478.2:n.676T>A (FKBP14)
NR_046479.2:n.432T>A (FKBP14)