Canonical Allele Identifier: CA1620985094

Gene: FKBP5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35639545A= , CM000668.2:g.35639545A=	GRCh38
NC_000006.11:g.35607322A= , CM000668.1:g.35607322A=	GRCh37
NC_000006.10:g.35715300A=	NCBI36
NG_012645.2:g.94039T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.106-2387T= MANE Select	ENSP00000349811.3:n.106-2387T=
ENST00000357266.8:c.106-2387T=	ENSP00000349811.3:n.106-2387T=
ENST00000536438.5:c.106-2387T=	ENSP00000444810.1:n.106-2387T=
ENST00000539068.5:c.106-2387T=	ENSP00000441205.1:n.106-2387T=
ENST00000542713.1:c.106-2387T=	ENSP00000442340.1:n.106-2387T=
NM_001145775.2:c.106-2387T=	NP_001139247.1:n.106-2387T=
NM_001145776.1:c.106-2387T=	NP_001139248.1:n.106-2387T=
NM_001145777.1:c.106-2387T=	NP_001139249.1:n.106-2387T=
NM_004117.3:c.106-2387T=	NP_004108.1:n.106-2387T=
XR_926743.1:n.287+5725A=
XR_002956345.1:n.1483-9805A=
NM_001145775.3:c.106-2387T=	NP_001139247.1:n.106-2387T=
NM_001145776.2:c.106-2387T=	NP_001139248.1:n.106-2387T=
NM_001145777.2:c.106-2387T=	NP_001139249.1:n.106-2387T=
NM_004117.4:c.106-2387T= MANE Select	NP_004108.1:n.106-2387T=