Canonical Allele Identifier: CA1620976847
Gene: FKBP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35624967T>A , CM000668.2:g.35624967T>A GRCh38
NC_000006.11:g.35592744T>A , CM000668.1:g.35592744T>A GRCh37
NC_000006.10:g.35700722T>A NCBI36
NG_012645.2:g.108617A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357266.9:c.251-4693A>T MANE Select ENSP00000349811.3:n.251-4693A>T
ENST00000357266.8:c.251-4693A>T ENSP00000349811.3:n.251-4693A>T
ENST00000536438.5:c.251-4693A>T ENSP00000444810.1:n.251-4693A>T
ENST00000539068.5:c.251-4693A>T ENSP00000441205.1:n.251-4693A>T
ENST00000542713.1:c.251-4693A>T ENSP00000442340.1:n.251-4693A>T
NM_001145775.2:c.251-4693A>T NP_001139247.1:n.251-4693A>T
NM_001145776.1:c.251-4693A>T NP_001139248.1:n.251-4693A>T
NM_001145777.1:c.251-4693A>T NP_001139249.1:n.251-4693A>T
NM_004117.3:c.251-4693A>T NP_004108.1:n.251-4693A>T
XR_002956345.1:n.1482+22644T>A
NM_001145775.3:c.251-4693A>T NP_001139247.1:n.251-4693A>T
NM_001145776.2:c.251-4693A>T NP_001139248.1:n.251-4693A>T
NM_001145777.2:c.251-4693A>T NP_001139249.1:n.251-4693A>T
NM_004117.4:c.251-4693A>T MANE Select NP_004108.1:n.251-4693A>T