Canonical Allele Identifier: CA2578595266
Gene: FKBP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35581829C>G , CM000668.2:g.35581829C>G GRCh38
NC_000006.11:g.35549606C>G , CM000668.1:g.35549606C>G GRCh37
NC_000006.10:g.35657584C>G NCBI36
NG_012645.2:g.151755G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000357266.9:c.841-1608G>C MANE Select ENSP00000349811.3:n.841-1608G>C
ENST00000357266.8:c.841-1608G>C ENSP00000349811.3:n.841-1608G>C
ENST00000536438.5:c.841-1608G>C ENSP00000444810.1:n.841-1608G>C
ENST00000539068.5:c.841-1608G>C ENSP00000441205.1:n.841-1608G>C
ENST00000542713.1:c.*5147G>C ENSP00000442340.1:n.*5147G>C
NM_001145775.2:c.841-1608G>C NP_001139247.1:n.841-1608G>C
NM_001145776.1:c.841-1608G>C NP_001139248.1:n.841-1608G>C
NM_001145777.1:c.*5147G>C NP_001139249.1:n.*5147G>C
NM_004117.3:c.841-1608G>C NP_004108.1:n.841-1608G>C
XR_242006.2:n.433-11201C>G
XR_242006.3:n.462-11201C>G
NM_001145775.3:c.841-1608G>C NP_001139247.1:n.841-1608G>C
NM_001145776.2:c.841-1608G>C NP_001139248.1:n.841-1608G>C
NM_001145777.2:c.*5147G>C NP_001139249.1:n.*5147G>C
NM_004117.4:c.841-1608G>C MANE Select NP_004108.1:n.841-1608G>C