Canonical Allele Identifier: CA367116878

Gene: FKBP14 FKBP14-AS1

Linked Data

• gnomAD v4: 7-30019083-A-C
• MyVariant Identifiers: chr7:g.30058699A>C (hg19) ; chr7:g.30019083A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019083A>C , CM000669.2:g.30019083A>C	GRCh38
NC_000007.13:g.30058699A>C , CM000669.1:g.30058699A>C	GRCh37
NC_000007.12:g.30025224A>C	NCBI36
NG_032173.1:g.12719T>G , LRG_454:g.12719T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.390T>G (FKBP14) MANE Select	ENSP00000222803.5:p.Asp130Glu
ENST00000222803.9:c.390T>G (FKBP14)	ENSP00000222803.5:p.Asp130Glu
ENST00000412494.1:c.393T>G (FKBP14)
ENST00000419018.1:c.*37T>G (FKBP14)	ENSP00000406270.1:n.*37T>G
NM_017946.3:c.390T>G , LRG_454t1:c.390T>G (FKBP14)	NP_060416.1:p.Asp130Glu
NR_046478.1:n.775T>G (FKBP14)
NR_046479.1:n.531T>G (FKBP14)
XR_927144.1:n.1570-6304A>C (FKBP14-AS1)
XR_927145.1:n.1139-6304A>C (FKBP14-AS1)
XR_927145.3:n.345-6304A>C (FKBP14-AS1)
NM_017946.4:c.390T>G (FKBP14) MANE Select	NP_060416.1:p.Asp130Glu
NR_046478.2:n.676T>G (FKBP14)
NR_046479.2:n.432T>G (FKBP14)