Canonical Allele Identifier: CA1620984880

Gene: FKBP5

Linked Data

• dbSNP Id: rs1764410345

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35639279_35639280del , CM000668.2:g.35639279_35639280del	GRCh38
NC_000006.11:g.35607056_35607057del , CM000668.1:g.35607056_35607057del	GRCh37
NC_000006.10:g.35715034_35715035del	NCBI36
NG_012645.2:g.94306_94307del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.106-2120_106-2119del MANE Select	ENSP00000349811.3:n.106-2120_106-2119del
ENST00000357266.8:c.106-2120_106-2119del	ENSP00000349811.3:n.106-2120_106-2119del
ENST00000536438.5:c.106-2120_106-2119del	ENSP00000444810.1:n.106-2120_106-2119del
ENST00000539068.5:c.106-2120_106-2119del	ENSP00000441205.1:n.106-2120_106-2119del
ENST00000542713.1:c.106-2120_106-2119del	ENSP00000442340.1:n.106-2120_106-2119del
NM_001145775.2:c.106-2120_106-2119del	NP_001139247.1:n.106-2120_106-2119del
NM_001145776.1:c.106-2120_106-2119del	NP_001139248.1:n.106-2120_106-2119del
NM_001145777.1:c.106-2120_106-2119del	NP_001139249.1:n.106-2120_106-2119del
NM_004117.3:c.106-2120_106-2119del	NP_004108.1:n.106-2120_106-2119del
XR_926743.1:n.287+5459_287+5460del
XR_002956345.1:n.1483-10071_1483-10070del
NM_001145775.3:c.106-2120_106-2119del	NP_001139247.1:n.106-2120_106-2119del
NM_001145776.2:c.106-2120_106-2119del	NP_001139248.1:n.106-2120_106-2119del
NM_001145777.2:c.106-2120_106-2119del	NP_001139249.1:n.106-2120_106-2119del
NM_004117.4:c.106-2120_106-2119del MANE Select	NP_004108.1:n.106-2120_106-2119del