Canonical Allele Identifier: CA2770632801
Gene: FKBP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35581810C>T , CM000668.2:g.35581810C>T GRCh38
NC_000006.11:g.35549587C>T , CM000668.1:g.35549587C>T GRCh37
NC_000006.10:g.35657565C>T NCBI36
NG_012645.2:g.151774G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357266.9:c.841-1589G>A MANE Select ENSP00000349811.3:n.841-1589G>A
ENST00000357266.8:c.841-1589G>A ENSP00000349811.3:n.841-1589G>A
ENST00000536438.5:c.841-1589G>A ENSP00000444810.1:n.841-1589G>A
ENST00000539068.5:c.841-1589G>A ENSP00000441205.1:n.841-1589G>A
ENST00000542713.1:c.*5166G>A ENSP00000442340.1:n.*5166G>A
NM_001145775.2:c.841-1589G>A NP_001139247.1:n.841-1589G>A
NM_001145776.1:c.841-1589G>A NP_001139248.1:n.841-1589G>A
NM_001145777.1:c.*5166G>A NP_001139249.1:n.*5166G>A
NM_004117.3:c.841-1589G>A NP_004108.1:n.841-1589G>A
XR_242006.2:n.433-11220C>T
XR_242006.3:n.462-11220C>T
NM_001145775.3:c.841-1589G>A NP_001139247.1:n.841-1589G>A
NM_001145776.2:c.841-1589G>A NP_001139248.1:n.841-1589G>A
NM_001145777.2:c.*5166G>A NP_001139249.1:n.*5166G>A
NM_004117.4:c.841-1589G>A MANE Select NP_004108.1:n.841-1589G>A