Canonical Allele Identifier: CA1620953686
Gene: FKBP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35581840A= , CM000668.2:g.35581840A= GRCh38
NC_000006.11:g.35549617A= , CM000668.1:g.35549617A= GRCh37
NC_000006.10:g.35657595A= NCBI36
NG_012645.2:g.151744T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357266.9:c.841-1619T= MANE Select ENSP00000349811.3:n.841-1619T=
ENST00000357266.8:c.841-1619T= ENSP00000349811.3:n.841-1619T=
ENST00000536438.5:c.841-1619T= ENSP00000444810.1:n.841-1619T=
ENST00000539068.5:c.841-1619T= ENSP00000441205.1:n.841-1619T=
ENST00000542713.1:c.*5136T= ENSP00000442340.1:n.*5136T=
NM_001145775.2:c.841-1619T= NP_001139247.1:n.841-1619T=
NM_001145776.1:c.841-1619T= NP_001139248.1:n.841-1619T=
NM_001145777.1:c.*5136T= NP_001139249.1:n.*5136T=
NM_004117.3:c.841-1619T= NP_004108.1:n.841-1619T=
XR_242006.2:n.433-11190A=
XR_242006.3:n.462-11190A=
NM_001145775.3:c.841-1619T= NP_001139247.1:n.841-1619T=
NM_001145776.2:c.841-1619T= NP_001139248.1:n.841-1619T=
NM_001145777.2:c.*5136T= NP_001139249.1:n.*5136T=
NM_004117.4:c.841-1619T= MANE Select NP_004108.1:n.841-1619T=