Canonical Allele Identifier: CA824248129

Gene: FKBP5

Linked Data

• dbSNP Id: rs1292889574
• MyVariant Identifiers: chr6:g.35607424del (hg19) ; chr6:g.35639647del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35639647del , CM000668.2:g.35639647del	GRCh38
NC_000006.11:g.35607424del , CM000668.1:g.35607424del	GRCh37
NC_000006.10:g.35715402del	NCBI36
NG_012645.2:g.93937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.106-2489del MANE Select	ENSP00000349811.3:n.106-2489del
ENST00000357266.8:c.106-2489del	ENSP00000349811.3:n.106-2489del
ENST00000536438.5:c.106-2489del	ENSP00000444810.1:n.106-2489del
ENST00000539068.5:c.106-2489del	ENSP00000441205.1:n.106-2489del
ENST00000542713.1:c.106-2489del	ENSP00000442340.1:n.106-2489del
NM_001145775.2:c.106-2489del	NP_001139247.1:n.106-2489del
NM_001145776.1:c.106-2489del	NP_001139248.1:n.106-2489del
NM_001145777.1:c.106-2489del	NP_001139249.1:n.106-2489del
NM_004117.3:c.106-2489del	NP_004108.1:n.106-2489del
XR_926743.1:n.287+5827del
XR_002956345.1:n.1483-9703del
NM_001145775.3:c.106-2489del	NP_001139247.1:n.106-2489del
NM_001145776.2:c.106-2489del	NP_001139248.1:n.106-2489del
NM_001145777.2:c.106-2489del	NP_001139249.1:n.106-2489del
NM_004117.4:c.106-2489del MANE Select	NP_004108.1:n.106-2489del