Canonical Allele Identifier: CA367116751

Gene: FKBP14 FKBP14-AS1

Linked Data

• dbSNP Id: rs1194280357
• gnomAD v4: 7-30019025-T-C
• MyVariant Identifiers: chr7:g.30058641T>C (hg19) ; chr7:g.30019025T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019025T>C , CM000669.2:g.30019025T>C	GRCh38
NC_000007.13:g.30058641T>C , CM000669.1:g.30058641T>C	GRCh37
NC_000007.12:g.30025166T>C	NCBI36
NG_032173.1:g.12777A>G , LRG_454:g.12777A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.448A>G (FKBP14) MANE Select	ENSP00000222803.5:p.Asn150Asp
ENST00000222803.9:c.448A>G (FKBP14)	ENSP00000222803.5:p.Asn150Asp
ENST00000412494.1:c.451A>G (FKBP14)
ENST00000419018.1:c.*95A>G (FKBP14)	ENSP00000406270.1:n.*95A>G
NM_017946.3:c.448A>G , LRG_454t1:c.448A>G (FKBP14)	NP_060416.1:p.Asn150Asp
NR_046478.1:n.833A>G (FKBP14)
NR_046479.1:n.589A>G (FKBP14)
XR_927144.1:n.1570-6362T>C (FKBP14-AS1)
XR_927145.1:n.1139-6362T>C (FKBP14-AS1)
XR_927145.3:n.345-6362T>C (FKBP14-AS1)
NM_017946.4:c.448A>G (FKBP14) MANE Select	NP_060416.1:p.Asn150Asp
NR_046478.2:n.734A>G (FKBP14)
NR_046479.2:n.490A>G (FKBP14)