Canonical Allele Identifier: CA367116943

Gene: FKBP14 FKBP14-AS1

Linked Data

• gnomAD v4: 7-30019111-G-T
• MyVariant Identifiers: chr7:g.30058727G>T (hg19) ; chr7:g.30019111G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019111G>T , CM000669.2:g.30019111G>T	GRCh38
NC_000007.13:g.30058727G>T , CM000669.1:g.30058727G>T	GRCh37
NC_000007.12:g.30025252G>T	NCBI36
NG_032173.1:g.12691C>A , LRG_454:g.12691C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.362C>A (FKBP14) MANE Select	ENSP00000222803.5:p.Pro121Gln
ENST00000222803.9:c.362C>A (FKBP14)	ENSP00000222803.5:p.Pro121Gln
ENST00000412494.1:c.365C>A (FKBP14)
ENST00000419018.1:c.*9C>A (FKBP14)	ENSP00000406270.1:n.*9C>A
NM_017946.3:c.362C>A , LRG_454t1:c.362C>A (FKBP14)	NP_060416.1:p.Pro121Gln
NR_046478.1:n.747C>A (FKBP14)
NR_046479.1:n.503C>A (FKBP14)
XR_927144.1:n.1570-6276G>T (FKBP14-AS1)
XR_927145.1:n.1139-6276G>T (FKBP14-AS1)
XR_927145.3:n.345-6276G>T (FKBP14-AS1)
NM_017946.4:c.362C>A (FKBP14) MANE Select	NP_060416.1:p.Pro121Gln
NR_046478.2:n.648C>A (FKBP14)
NR_046479.2:n.404C>A (FKBP14)