Canonical Allele Identifier: CA367116928

Gene: FKBP14 FKBP14-AS1

Linked Data

• gnomAD v4: 7-30019105-C-G
• MyVariant Identifiers: chr7:g.30058721C>G (hg19) ; chr7:g.30019105C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019105C>G , CM000669.2:g.30019105C>G	GRCh38
NC_000007.13:g.30058721C>G , CM000669.1:g.30058721C>G	GRCh37
NC_000007.12:g.30025246C>G	NCBI36
NG_032173.1:g.12697G>C , LRG_454:g.12697G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.368G>C (FKBP14) MANE Select	ENSP00000222803.5:p.Ser123Thr
ENST00000222803.9:c.368G>C (FKBP14)	ENSP00000222803.5:p.Ser123Thr
ENST00000412494.1:c.371G>C (FKBP14)
ENST00000419018.1:c.*15G>C (FKBP14)	ENSP00000406270.1:n.*15G>C
NM_017946.3:c.368G>C , LRG_454t1:c.368G>C (FKBP14)	NP_060416.1:p.Ser123Thr
NR_046478.1:n.753G>C (FKBP14)
NR_046479.1:n.509G>C (FKBP14)
XR_927144.1:n.1570-6282C>G (FKBP14-AS1)
XR_927145.1:n.1139-6282C>G (FKBP14-AS1)
XR_927145.3:n.345-6282C>G (FKBP14-AS1)
NM_017946.4:c.368G>C (FKBP14) MANE Select	NP_060416.1:p.Ser123Thr
NR_046478.2:n.654G>C (FKBP14)
NR_046479.2:n.410G>C (FKBP14)