Canonical Allele Identifier: CA2678420247

Gene: FKBP5

Linked Data

• gnomAD v4: 6-35581827-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35581827G>A , CM000668.2:g.35581827G>A	GRCh38
NC_000006.11:g.35549604G>A , CM000668.1:g.35549604G>A	GRCh37
NC_000006.10:g.35657582G>A	NCBI36
NG_012645.2:g.151757C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000357266.9:c.841-1606C>T MANE Select	ENSP00000349811.3:n.841-1606C>T
ENST00000357266.8:c.841-1606C>T	ENSP00000349811.3:n.841-1606C>T
ENST00000536438.5:c.841-1606C>T	ENSP00000444810.1:n.841-1606C>T
ENST00000539068.5:c.841-1606C>T	ENSP00000441205.1:n.841-1606C>T
ENST00000542713.1:c.*5149C>T	ENSP00000442340.1:n.*5149C>T
NM_001145775.2:c.841-1606C>T	NP_001139247.1:n.841-1606C>T
NM_001145776.1:c.841-1606C>T	NP_001139248.1:n.841-1606C>T
NM_001145777.1:c.*5149C>T	NP_001139249.1:n.*5149C>T
NM_004117.3:c.841-1606C>T	NP_004108.1:n.841-1606C>T
XR_242006.2:n.433-11203G>A
XR_242006.3:n.462-11203G>A
NM_001145775.3:c.841-1606C>T	NP_001139247.1:n.841-1606C>T
NM_001145776.2:c.841-1606C>T	NP_001139248.1:n.841-1606C>T
NM_001145777.2:c.*5149C>T	NP_001139249.1:n.*5149C>T
NM_004117.4:c.841-1606C>T MANE Select	NP_004108.1:n.841-1606C>T