Canonical Allele Identifier: CA2678420232

Gene: FKBP5

Linked Data

• gnomAD v4: 6-35581794-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35581794G>T , CM000668.2:g.35581794G>T	GRCh38
NC_000006.11:g.35549571G>T , CM000668.1:g.35549571G>T	GRCh37
NC_000006.10:g.35657549G>T	NCBI36
NG_012645.2:g.151790C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357266.9:c.841-1573C>A MANE Select	ENSP00000349811.3:n.841-1573C>A
ENST00000357266.8:c.841-1573C>A	ENSP00000349811.3:n.841-1573C>A
ENST00000536438.5:c.841-1573C>A	ENSP00000444810.1:n.841-1573C>A
ENST00000539068.5:c.841-1573C>A	ENSP00000441205.1:n.841-1573C>A
ENST00000542713.1:c.*5182C>A	ENSP00000442340.1:n.*5182C>A
NM_001145775.2:c.841-1573C>A	NP_001139247.1:n.841-1573C>A
NM_001145776.1:c.841-1573C>A	NP_001139248.1:n.841-1573C>A
NM_001145777.1:c.*5182C>A	NP_001139249.1:n.*5182C>A
NM_004117.3:c.841-1573C>A	NP_004108.1:n.841-1573C>A
XR_242006.2:n.433-11236G>T
XR_242006.3:n.462-11236G>T
NM_001145775.3:c.841-1573C>A	NP_001139247.1:n.841-1573C>A
NM_001145776.2:c.841-1573C>A	NP_001139248.1:n.841-1573C>A
NM_001145777.2:c.*5182C>A	NP_001139249.1:n.*5182C>A
NM_004117.4:c.841-1573C>A MANE Select	NP_004108.1:n.841-1573C>A