Canonical Allele Identifier: CA1620969658
Gene: FKBP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35599305A= , CM000668.2:g.35599305A= GRCh38
NC_000006.11:g.35567082A= , CM000668.1:g.35567082A= GRCh37
NC_000006.10:g.35675060A= NCBI36
NG_012645.2:g.134279T=

Transcript Alleles

HGVS Amino-acid Change
NM_004117.4:c.509-1901T= MANE Select NP_004108.1:n.509-1901T=
ENST00000357266.9:c.509-1901T= MANE Select ENSP00000349811.3:n.509-1901T=
NM_001145775.2:c.509-1901T= NP_001139247.1:n.509-1901T=
NM_001145775.3:c.509-1901T= NP_001139247.1:n.509-1901T=
NM_001145776.1:c.509-1901T= NP_001139248.1:n.509-1901T=
NM_001145776.2:c.509-1901T= NP_001139248.1:n.509-1901T=
NM_001145777.1:c.509-1901T= NP_001139249.1:n.509-1901T=
NM_001145777.2:c.509-1901T= NP_001139249.1:n.509-1901T=
NM_004117.3:c.509-1901T= NP_004108.1:n.509-1901T=
ENST00000357266.8:c.509-1901T= ENSP00000349811.3:n.509-1901T=
ENST00000536438.5:c.509-1901T= ENSP00000444810.1:n.509-1901T=
ENST00000539068.5:c.509-1901T= ENSP00000441205.1:n.509-1901T=
ENST00000542713.1:c.509-1901T= ENSP00000442340.1:n.509-1901T=