Canonical Allele Identifier: CA367116785

Gene: FKBP14 FKBP14-AS1

Linked Data

• dbSNP Id: rs1789963225
• MyVariant Identifiers: chr7:g.30058655T>G (hg19) ; chr7:g.30019039T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019039T>G , CM000669.2:g.30019039T>G	GRCh38
NC_000007.13:g.30058655T>G , CM000669.1:g.30058655T>G	GRCh37
NC_000007.12:g.30025180T>G	NCBI36
NG_032173.1:g.12763A>C , LRG_454:g.12763A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.434A>C (FKBP14) MANE Select	ENSP00000222803.5:p.Gln145Pro
ENST00000222803.9:c.434A>C (FKBP14)	ENSP00000222803.5:p.Gln145Pro
ENST00000412494.1:c.437A>C (FKBP14)
ENST00000419018.1:c.*81A>C (FKBP14)	ENSP00000406270.1:n.*81A>C
NM_017946.3:c.434A>C , LRG_454t1:c.434A>C (FKBP14)	NP_060416.1:p.Gln145Pro
NR_046478.1:n.819A>C (FKBP14)
NR_046479.1:n.575A>C (FKBP14)
XR_927144.1:n.1570-6348T>G (FKBP14-AS1)
XR_927145.1:n.1139-6348T>G (FKBP14-AS1)
XR_927145.3:n.345-6348T>G (FKBP14-AS1)
NM_017946.4:c.434A>C (FKBP14) MANE Select	NP_060416.1:p.Gln145Pro
NR_046478.2:n.720A>C (FKBP14)
NR_046479.2:n.476A>C (FKBP14)