Canonical Allele Identifier: CA367116906

Gene: FKBP14 FKBP14-AS1

Linked Data

• dbSNP Id: rs1789964580
• MyVariant Identifiers: chr7:g.30058710A>C (hg19) ; chr7:g.30019094A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019094A>C , CM000669.2:g.30019094A>C	GRCh38
NC_000007.13:g.30058710A>C , CM000669.1:g.30058710A>C	GRCh37
NC_000007.12:g.30025235A>C	NCBI36
NG_032173.1:g.12708T>G , LRG_454:g.12708T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.379T>G (FKBP14) MANE Select	ENSP00000222803.5:p.Phe127Val
ENST00000222803.9:c.379T>G (FKBP14)	ENSP00000222803.5:p.Phe127Val
ENST00000412494.1:c.382T>G (FKBP14)
ENST00000419018.1:c.*26T>G (FKBP14)	ENSP00000406270.1:n.*26T>G
NM_017946.3:c.379T>G , LRG_454t1:c.379T>G (FKBP14)	NP_060416.1:p.Phe127Val
NR_046478.1:n.764T>G (FKBP14)
NR_046479.1:n.520T>G (FKBP14)
XR_927144.1:n.1570-6293A>C (FKBP14-AS1)
XR_927145.1:n.1139-6293A>C (FKBP14-AS1)
XR_927145.3:n.345-6293A>C (FKBP14-AS1)
NM_017946.4:c.379T>G (FKBP14) MANE Select	NP_060416.1:p.Phe127Val
NR_046478.2:n.665T>G (FKBP14)
NR_046479.2:n.421T>G (FKBP14)