Canonical Allele Identifier: CA454237137

Gene: FKBP14 FKBP14-AS1

Linked Data

• ClinVar Variation Id: 1970914
• ClinVar RCV Id: RCV002735640
• dbSNP Id: rs1789965716
• gnomAD v4: 7-30019122-A-G
• MyVariant Identifiers: chr7:g.30058738A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019122A>G , CM000669.2:g.30019122A>G	GRCh38
NC_000007.13:g.30058738A>G , CM000669.1:g.30058738A>G	GRCh37
NC_000007.12:g.30025263A>G	NCBI36
NG_032173.1:g.12680T>C , LRG_454:g.12680T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.351T>C (FKBP14) MANE Select	ENSP00000222803.5:p.Gly117=
ENST00000222803.9:c.351T>C (FKBP14)	ENSP00000222803.5:p.Gly117=
ENST00000412494.1:c.354T>C (FKBP14)
ENST00000419018.1:c.199T>C (FKBP14)	ENSP00000406270.1:p.Ter67Gln
NM_017946.3:c.351T>C , LRG_454t1:c.351T>C (FKBP14)	NP_060416.1:p.Gly117=
NR_046478.1:n.736T>C (FKBP14)
NR_046479.1:n.492T>C (FKBP14)
XR_927144.1:n.1570-6265A>G (FKBP14-AS1)
XR_927145.1:n.1139-6265A>G (FKBP14-AS1)
XR_927145.3:n.345-6265A>G (FKBP14-AS1)
NM_017946.4:c.351T>C (FKBP14) MANE Select	NP_060416.1:p.Gly117=
NR_046478.2:n.637T>C (FKBP14)
NR_046479.2:n.393T>C (FKBP14)