Canonical Allele Identifier: CA1620953669

Gene: FKBP5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35581800C= , CM000668.2:g.35581800C=	GRCh38
NC_000006.11:g.35549577C= , CM000668.1:g.35549577C=	GRCh37
NC_000006.10:g.35657555C=	NCBI36
NG_012645.2:g.151784G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000357266.9:c.841-1579G= MANE Select	ENSP00000349811.3:n.841-1579G=
ENST00000357266.8:c.841-1579G=	ENSP00000349811.3:n.841-1579G=
ENST00000536438.5:c.841-1579G=	ENSP00000444810.1:n.841-1579G=
ENST00000539068.5:c.841-1579G=	ENSP00000441205.1:n.841-1579G=
ENST00000542713.1:c.*5176G=	ENSP00000442340.1:n.*5176G=
NM_001145775.2:c.841-1579G=	NP_001139247.1:n.841-1579G=
NM_001145776.1:c.841-1579G=	NP_001139248.1:n.841-1579G=
NM_001145777.1:c.*5176G=	NP_001139249.1:n.*5176G=
NM_004117.3:c.841-1579G=	NP_004108.1:n.841-1579G=
XR_242006.2:n.433-11230C=
XR_242006.3:n.462-11230C=
NM_001145775.3:c.841-1579G=	NP_001139247.1:n.841-1579G=
NM_001145776.2:c.841-1579G=	NP_001139248.1:n.841-1579G=
NM_001145777.2:c.*5176G=	NP_001139249.1:n.*5176G=
NM_004117.4:c.841-1579G= MANE Select	NP_004108.1:n.841-1579G=