Canonical Allele Identifier: CA454237083
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.30058660T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30019044T>G , CM000669.2:g.30019044T>G GRCh38
NC_000007.13:g.30058660T>G , CM000669.1:g.30058660T>G GRCh37
NC_000007.12:g.30025185T>G NCBI36
NG_032173.1:g.12758A>C , LRG_454:g.12758A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222803.10:c.429A>C (FKBP14) MANE Select ENSP00000222803.5:p.Ser143=
ENST00000222803.9:c.429A>C (FKBP14) ENSP00000222803.5:p.Ser143=
ENST00000412494.1:c.432A>C (FKBP14)
ENST00000419018.1:c.*76A>C (FKBP14) ENSP00000406270.1:n.*76A>C
NM_017946.3:c.429A>C , LRG_454t1:c.429A>C (FKBP14) NP_060416.1:p.Ser143=
NR_046478.1:n.814A>C (FKBP14)
NR_046479.1:n.570A>C (FKBP14)
XR_927144.1:n.1570-6343T>G (FKBP14-AS1)
XR_927145.1:n.1139-6343T>G (FKBP14-AS1)
XR_927145.3:n.345-6343T>G (FKBP14-AS1)
NM_017946.4:c.429A>C (FKBP14) MANE Select NP_060416.1:p.Ser143=
NR_046478.2:n.715A>C (FKBP14)
NR_046479.2:n.471A>C (FKBP14)