Canonical Allele Identifier: CA2678420250
Gene: FKBP5 HGNC NCBI

Linked Data

gnomAD v4: 6-35581830-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35581830C>T , CM000668.2:g.35581830C>T GRCh38
NC_000006.11:g.35549607C>T , CM000668.1:g.35549607C>T GRCh37
NC_000006.10:g.35657585C>T NCBI36
NG_012645.2:g.151754G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357266.9:c.841-1609G>A MANE Select ENSP00000349811.3:n.841-1609G>A
ENST00000357266.8:c.841-1609G>A ENSP00000349811.3:n.841-1609G>A
ENST00000536438.5:c.841-1609G>A ENSP00000444810.1:n.841-1609G>A
ENST00000539068.5:c.841-1609G>A ENSP00000441205.1:n.841-1609G>A
ENST00000542713.1:c.*5146G>A ENSP00000442340.1:n.*5146G>A
NM_001145775.2:c.841-1609G>A NP_001139247.1:n.841-1609G>A
NM_001145776.1:c.841-1609G>A NP_001139248.1:n.841-1609G>A
NM_001145777.1:c.*5146G>A NP_001139249.1:n.*5146G>A
NM_004117.3:c.841-1609G>A NP_004108.1:n.841-1609G>A
XR_242006.2:n.433-11200C>T
XR_242006.3:n.462-11200C>T
NM_001145775.3:c.841-1609G>A NP_001139247.1:n.841-1609G>A
NM_001145776.2:c.841-1609G>A NP_001139248.1:n.841-1609G>A
NM_001145777.2:c.*5146G>A NP_001139249.1:n.*5146G>A
NM_004117.4:c.841-1609G>A MANE Select NP_004108.1:n.841-1609G>A