Canonical Allele Identifier: CA367116871

Gene: FKBP14 FKBP14-AS1

Linked Data

• MyVariant Identifiers: chr7:g.30058695G>T (hg19) ; chr7:g.30019079G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019079G>T , CM000669.2:g.30019079G>T	GRCh38
NC_000007.13:g.30058695G>T , CM000669.1:g.30058695G>T	GRCh37
NC_000007.12:g.30025220G>T	NCBI36
NG_032173.1:g.12723C>A , LRG_454:g.12723C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.394C>A (FKBP14) MANE Select	ENSP00000222803.5:p.Leu132Met
ENST00000222803.9:c.394C>A (FKBP14)	ENSP00000222803.5:p.Leu132Met
ENST00000412494.1:c.397C>A (FKBP14)
ENST00000419018.1:c.*41C>A (FKBP14)	ENSP00000406270.1:n.*41C>A
NM_017946.3:c.394C>A , LRG_454t1:c.394C>A (FKBP14)	NP_060416.1:p.Leu132Met
NR_046478.1:n.779C>A (FKBP14)
NR_046479.1:n.535C>A (FKBP14)
XR_927144.1:n.1570-6308G>T (FKBP14-AS1)
XR_927145.1:n.1139-6308G>T (FKBP14-AS1)
XR_927145.3:n.345-6308G>T (FKBP14-AS1)
NM_017946.4:c.394C>A (FKBP14) MANE Select	NP_060416.1:p.Leu132Met
NR_046478.2:n.680C>A (FKBP14)
NR_046479.2:n.436C>A (FKBP14)