Canonical Allele Identifier: CA1620985283

Gene: FKBP5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35639827C= , CM000668.2:g.35639827C=	GRCh38
NC_000006.11:g.35607604C= , CM000668.1:g.35607604C=	GRCh37
NC_000006.10:g.35715582C=	NCBI36
NG_012645.2:g.93757G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000357266.9:c.106-2669G= MANE Select	ENSP00000349811.3:n.106-2669G=
ENST00000357266.8:c.106-2669G=	ENSP00000349811.3:n.106-2669G=
ENST00000536438.5:c.106-2669G=	ENSP00000444810.1:n.106-2669G=
ENST00000539068.5:c.106-2669G=	ENSP00000441205.1:n.106-2669G=
ENST00000542713.1:c.106-2669G=	ENSP00000442340.1:n.106-2669G=
NM_001145775.2:c.106-2669G=	NP_001139247.1:n.106-2669G=
NM_001145776.1:c.106-2669G=	NP_001139248.1:n.106-2669G=
NM_001145777.1:c.106-2669G=	NP_001139249.1:n.106-2669G=
NM_004117.3:c.106-2669G=	NP_004108.1:n.106-2669G=
XR_926743.1:n.287+6007C=
XR_002956345.1:n.1483-9523C=
NM_001145775.3:c.106-2669G=	NP_001139247.1:n.106-2669G=
NM_001145776.2:c.106-2669G=	NP_001139248.1:n.106-2669G=
NM_001145777.2:c.106-2669G=	NP_001139249.1:n.106-2669G=
NM_004117.4:c.106-2669G= MANE Select	NP_004108.1:n.106-2669G=