Canonical Allele Identifier: CA367116815

Gene: FKBP14 FKBP14-AS1

Linked Data

• MyVariant Identifiers: chr7:g.30058668G>C (hg19) ; chr7:g.30019052G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019052G>C , CM000669.2:g.30019052G>C	GRCh38
NC_000007.13:g.30058668G>C , CM000669.1:g.30058668G>C	GRCh37
NC_000007.12:g.30025193G>C	NCBI36
NG_032173.1:g.12750C>G , LRG_454:g.12750C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.421C>G (FKBP14) MANE Select	ENSP00000222803.5:p.His141Asp
ENST00000222803.9:c.421C>G (FKBP14)	ENSP00000222803.5:p.His141Asp
ENST00000412494.1:c.424C>G (FKBP14)
ENST00000419018.1:c.*68C>G (FKBP14)	ENSP00000406270.1:n.*68C>G
NM_017946.3:c.421C>G , LRG_454t1:c.421C>G (FKBP14)	NP_060416.1:p.His141Asp
NR_046478.1:n.806C>G (FKBP14)
NR_046479.1:n.562C>G (FKBP14)
XR_927144.1:n.1570-6335G>C (FKBP14-AS1)
XR_927145.1:n.1139-6335G>C (FKBP14-AS1)
XR_927145.3:n.345-6335G>C (FKBP14-AS1)
NM_017946.4:c.421C>G (FKBP14) MANE Select	NP_060416.1:p.His141Asp
NR_046478.2:n.707C>G (FKBP14)
NR_046479.2:n.463C>G (FKBP14)