Canonical Allele Identifier: CA367116756

Gene: FKBP14 FKBP14-AS1

Linked Data

• ClinVar Variation Id: 1063669
• ClinVar RCV Id: RCV001373526
• dbSNP Id: rs2127948264
• MyVariant Identifiers: chr7:g.30058644G>C (hg19) ; chr7:g.30019028G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019028G>C , CM000669.2:g.30019028G>C	GRCh38
NC_000007.13:g.30058644G>C , CM000669.1:g.30058644G>C	GRCh37
NC_000007.12:g.30025169G>C	NCBI36
NG_032173.1:g.12774C>G , LRG_454:g.12774C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.445C>G (FKBP14) MANE Select	ENSP00000222803.5:p.Leu149Val
ENST00000222803.9:c.445C>G (FKBP14)	ENSP00000222803.5:p.Leu149Val
ENST00000412494.1:c.448C>G (FKBP14)
ENST00000419018.1:c.*92C>G (FKBP14)	ENSP00000406270.1:n.*92C>G
NM_017946.3:c.445C>G , LRG_454t1:c.445C>G (FKBP14)	NP_060416.1:p.Leu149Val
NR_046478.1:n.830C>G (FKBP14)
NR_046479.1:n.586C>G (FKBP14)
XR_927144.1:n.1570-6359G>C (FKBP14-AS1)
XR_927145.1:n.1139-6359G>C (FKBP14-AS1)
XR_927145.3:n.345-6359G>C (FKBP14-AS1)
NM_017946.4:c.445C>G (FKBP14) MANE Select	NP_060416.1:p.Leu149Val
NR_046478.2:n.731C>G (FKBP14)
NR_046479.2:n.487C>G (FKBP14)