Canonical Allele Identifier: CA1620993037
Gene: FKBP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35654004G= , CM000668.2:g.35654004G= GRCh38
NC_000006.11:g.35621781G= , CM000668.1:g.35621781G= GRCh37
NC_000006.10:g.35729759G= NCBI36
NG_012645.2:g.79580C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357266.9:c.-19-11161C= MANE Select ENSP00000349811.3:n.-19-11161C=
ENST00000357266.8:c.-19-11161C= ENSP00000349811.3:n.-19-11161C=
ENST00000536438.5:c.-19-11161C= ENSP00000444810.1:n.-19-11161C=
ENST00000539068.5:c.-19-11161C= ENSP00000441205.1:n.-19-11161C=
ENST00000542713.1:c.-19-11161C= ENSP00000442340.1:n.-19-11161C=
NM_001145775.2:c.-19-11161C= NP_001139247.1:n.-19-11161C=
NM_001145776.1:c.-19-11161C= NP_001139248.1:n.-19-11161C=
NM_001145777.1:c.-19-11161C= NP_001139249.1:n.-19-11161C=
NM_004117.3:c.-19-11161C= NP_004108.1:n.-19-11161C=
NM_001145775.3:c.-19-11161C= NP_001139247.1:n.-19-11161C=
NM_001145776.2:c.-19-11161C= NP_001139248.1:n.-19-11161C=
NM_001145777.2:c.-19-11161C= NP_001139249.1:n.-19-11161C=
NM_004117.4:c.-19-11161C= MANE Select NP_004108.1:n.-19-11161C=