Canonical Allele Identifier: CA367116868

Gene: FKBP14 FKBP14-AS1

Linked Data

• COSMIC: COSM5895901
• MyVariant Identifiers: chr7:g.30058694A>G (hg19) ; chr7:g.30019078A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019078A>G , CM000669.2:g.30019078A>G	GRCh38
NC_000007.13:g.30058694A>G , CM000669.1:g.30058694A>G	GRCh37
NC_000007.12:g.30025219A>G	NCBI36
NG_032173.1:g.12724T>C , LRG_454:g.12724T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.395T>C (FKBP14) MANE Select	ENSP00000222803.5:p.Leu132Pro
ENST00000222803.9:c.395T>C (FKBP14)	ENSP00000222803.5:p.Leu132Pro
ENST00000412494.1:c.398T>C (FKBP14)
ENST00000419018.1:c.*42T>C (FKBP14)	ENSP00000406270.1:n.*42T>C
NM_017946.3:c.395T>C , LRG_454t1:c.395T>C (FKBP14)	NP_060416.1:p.Leu132Pro
NR_046478.1:n.780T>C (FKBP14)
NR_046479.1:n.536T>C (FKBP14)
XR_927144.1:n.1570-6309A>G (FKBP14-AS1)
XR_927145.1:n.1139-6309A>G (FKBP14-AS1)
XR_927145.3:n.345-6309A>G (FKBP14-AS1)
NM_017946.4:c.395T>C (FKBP14) MANE Select	NP_060416.1:p.Leu132Pro
NR_046478.2:n.681T>C (FKBP14)
NR_046479.2:n.437T>C (FKBP14)