Canonical Allele Identifier: CA2678420241
Gene: FKBP5 HGNC NCBI

Linked Data

gnomAD v4: 6-35581818-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35581818T>C , CM000668.2:g.35581818T>C GRCh38
NC_000006.11:g.35549595T>C , CM000668.1:g.35549595T>C GRCh37
NC_000006.10:g.35657573T>C NCBI36
NG_012645.2:g.151766A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000357266.9:c.841-1597A>G MANE Select ENSP00000349811.3:n.841-1597A>G
ENST00000357266.8:c.841-1597A>G ENSP00000349811.3:n.841-1597A>G
ENST00000536438.5:c.841-1597A>G ENSP00000444810.1:n.841-1597A>G
ENST00000539068.5:c.841-1597A>G ENSP00000441205.1:n.841-1597A>G
ENST00000542713.1:c.*5158A>G ENSP00000442340.1:n.*5158A>G
NM_001145775.2:c.841-1597A>G NP_001139247.1:n.841-1597A>G
NM_001145776.1:c.841-1597A>G NP_001139248.1:n.841-1597A>G
NM_001145777.1:c.*5158A>G NP_001139249.1:n.*5158A>G
NM_004117.3:c.841-1597A>G NP_004108.1:n.841-1597A>G
XR_242006.2:n.433-11212T>C
XR_242006.3:n.462-11212T>C
NM_001145775.3:c.841-1597A>G NP_001139247.1:n.841-1597A>G
NM_001145776.2:c.841-1597A>G NP_001139248.1:n.841-1597A>G
NM_001145777.2:c.*5158A>G NP_001139249.1:n.*5158A>G
NM_004117.4:c.841-1597A>G MANE Select NP_004108.1:n.841-1597A>G