Canonical Allele Identifier: CA837448836

Gene: FKBP14 FKBP14-AS1

Linked Data

• dbSNP Id: rs1381468787
• gnomAD v4: 7-30019200-A-C
• MyVariant Identifiers: chr7:g.30058816A>C (hg19) ; chr7:g.30019200A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30019200A>C , CM000669.2:g.30019200A>C	GRCh38
NC_000007.13:g.30058816A>C , CM000669.1:g.30058816A>C	GRCh37
NC_000007.12:g.30025341A>C	NCBI36
NG_032173.1:g.12602T>G , LRG_454:g.12602T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222803.10:c.350-77T>G (FKBP14) MANE Select	ENSP00000222803.5:n.350-77T>G
ENST00000222803.9:c.350-77T>G (FKBP14)	ENSP00000222803.5:n.350-77T>G
ENST00000412494.1:c.353-77T>G (FKBP14)
ENST00000419018.1:c.198-77T>G (FKBP14)	ENSP00000406270.1:n.198-77T>G
NM_017946.3:c.350-77T>G , LRG_454t1:c.350-77T>G (FKBP14)	NP_060416.1:n.350-77T>G
NR_046478.1:n.735-77T>G (FKBP14)
NR_046479.1:n.491-77T>G (FKBP14)
XR_927144.1:n.1570-6187A>C (FKBP14-AS1)
XR_927145.1:n.1139-6187A>C (FKBP14-AS1)
XR_927145.3:n.345-6187A>C (FKBP14-AS1)
NM_017946.4:c.350-77T>G (FKBP14) MANE Select	NP_060416.1:n.350-77T>G
NR_046478.2:n.636-77T>G (FKBP14)
NR_046479.2:n.392-77T>G (FKBP14)