Canonical Allele Identifier: CA137263695

Gene: FKBP5

Linked Data

• dbSNP Id: rs1049269607
• MyVariant Identifiers: chr6:g.35607117del (hg19) ; chr6:g.35639340del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35639343del , CM000668.2:g.35639343del	GRCh38
NC_000006.11:g.35607120del , CM000668.1:g.35607120del	GRCh37
NC_000006.10:g.35715098del	NCBI36
NG_012645.2:g.94244del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.106-2182del MANE Select	ENSP00000349811.3:n.106-2182del
ENST00000357266.8:c.106-2182del	ENSP00000349811.3:n.106-2182del
ENST00000536438.5:c.106-2182del	ENSP00000444810.1:n.106-2182del
ENST00000539068.5:c.106-2182del	ENSP00000441205.1:n.106-2182del
ENST00000542713.1:c.106-2182del	ENSP00000442340.1:n.106-2182del
NM_001145775.2:c.106-2182del	NP_001139247.1:n.106-2182del
NM_001145776.1:c.106-2182del	NP_001139248.1:n.106-2182del
NM_001145777.1:c.106-2182del	NP_001139249.1:n.106-2182del
NM_004117.3:c.106-2182del	NP_004108.1:n.106-2182del
XR_926743.1:n.287+5523del
XR_002956345.1:n.1483-10007del
NM_001145775.3:c.106-2182del	NP_001139247.1:n.106-2182del
NM_001145776.2:c.106-2182del	NP_001139248.1:n.106-2182del
NM_001145777.2:c.106-2182del	NP_001139249.1:n.106-2182del
NM_004117.4:c.106-2182del MANE Select	NP_004108.1:n.106-2182del