Canonical Allele Identifier: CA367116781

Gene: FKBP14 FKBP14-AS1

Linked Data

• MyVariant Identifiers: chr7:g.30058654T>G (hg19) ; chr7:g.30019038T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019038T>G , CM000669.2:g.30019038T>G	GRCh38
NC_000007.13:g.30058654T>G , CM000669.1:g.30058654T>G	GRCh37
NC_000007.12:g.30025179T>G	NCBI36
NG_032173.1:g.12764A>C , LRG_454:g.12764A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.435A>C (FKBP14) MANE Select	ENSP00000222803.5:p.Gln145His
ENST00000222803.9:c.435A>C (FKBP14)	ENSP00000222803.5:p.Gln145His
ENST00000412494.1:c.438A>C (FKBP14)
ENST00000419018.1:c.*82A>C (FKBP14)	ENSP00000406270.1:n.*82A>C
NM_017946.3:c.435A>C , LRG_454t1:c.435A>C (FKBP14)	NP_060416.1:p.Gln145His
NR_046478.1:n.820A>C (FKBP14)
NR_046479.1:n.576A>C (FKBP14)
XR_927144.1:n.1570-6349T>G (FKBP14-AS1)
XR_927145.1:n.1139-6349T>G (FKBP14-AS1)
XR_927145.3:n.345-6349T>G (FKBP14-AS1)
NM_017946.4:c.435A>C (FKBP14) MANE Select	NP_060416.1:p.Gln145His
NR_046478.2:n.721A>C (FKBP14)
NR_046479.2:n.477A>C (FKBP14)