Canonical Allele Identifier: CA1620977996
Gene: FKBP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35611153T= , CM000668.2:g.35611153T= GRCh38
NC_000006.11:g.35578930T= , CM000668.1:g.35578930T= GRCh37
NC_000006.10:g.35686908T= NCBI36
NG_012645.2:g.122431A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357266.9:c.508+7943A= MANE Select ENSP00000349811.3:n.508+7943A=
ENST00000357266.8:c.508+7943A= ENSP00000349811.3:n.508+7943A=
ENST00000536438.5:c.508+7943A= ENSP00000444810.1:n.508+7943A=
ENST00000539068.5:c.508+7943A= ENSP00000441205.1:n.508+7943A=
ENST00000542713.1:c.508+7943A= ENSP00000442340.1:n.508+7943A=
NM_001145775.2:c.508+7943A= NP_001139247.1:n.508+7943A=
NM_001145776.1:c.508+7943A= NP_001139248.1:n.508+7943A=
NM_001145777.1:c.508+7943A= NP_001139249.1:n.508+7943A=
NM_004117.3:c.508+7943A= NP_004108.1:n.508+7943A=
XR_926744.1:n.1937-3528T=
XR_002956345.1:n.1482+8830T=
NM_001145775.3:c.508+7943A= NP_001139247.1:n.508+7943A=
NM_001145776.2:c.508+7943A= NP_001139248.1:n.508+7943A=
NM_001145777.2:c.508+7943A= NP_001139249.1:n.508+7943A=
NM_004117.4:c.508+7943A= MANE Select NP_004108.1:n.508+7943A=