Canonical Allele Identifier: CA4203436
Community Standard Title: NM_017946.4(FKBP14):c.333T>C (p.Tyr111=)
Gene: FKBP14 HGNC NCBI
FKBP14-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30022681A>G , CM000669.2:g.30022681A>G GRCh38
NC_000007.13:g.30062297A>G , CM000669.1:g.30062297A>G GRCh37
NC_000007.12:g.30028822A>G NCBI36
NG_032173.1:g.9121T>C , LRG_454:g.9121T>C

Transcript Alleles

HGVS Amino-acid Change
NM_017946.4:c.333T>C (FKBP14) MANE Select NP_060416.1:p.Tyr111=
ENST00000222803.10:c.333T>C (FKBP14) MANE Select ENSP00000222803.5:p.Tyr111=
NM_017946.3:c.333T>C , LRG_454t1:c.333T>C (FKBP14) NP_060416.1:p.Tyr111=
NR_046478.1:n.626T>C (FKBP14)
NR_046478.2:n.527T>C (FKBP14)
NR_046479.1:n.491-3558T>C (FKBP14)
NR_046479.2:n.392-3558T>C (FKBP14)
ENST00000222803.9:c.333T>C (FKBP14) ENSP00000222803.5:p.Tyr111=
ENST00000412494.1:c.244T>C (FKBP14)
ENST00000419018.1:c.198-3558T>C (FKBP14) ENSP00000406270.1:n.198-3558T>C
ENST00000479939.1:n.461T>C (FKBP14)
XR_927144.1:n.1570-2706A>G (FKBP14-AS1)
XR_927145.1:n.1139-2706A>G (FKBP14-AS1)
XR_927145.3:n.345-2706A>G (FKBP14-AS1)