Canonical Allele Identifier: CA824229027

Gene: FKBP5

Linked Data

• dbSNP Id: rs1246696691
• gnomAD v3: 6-35581834-A-G
• gnomAD v4: 6-35581834-A-G
• MyVariant Identifiers: chr6:g.35549611A>G (hg19) ; chr6:g.35581834A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35581834A>G , CM000668.2:g.35581834A>G	GRCh38
NC_000006.11:g.35549611A>G , CM000668.1:g.35549611A>G	GRCh37
NC_000006.10:g.35657589A>G	NCBI36
NG_012645.2:g.151750T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000357266.9:c.841-1613T>C MANE Select	ENSP00000349811.3:n.841-1613T>C
ENST00000357266.8:c.841-1613T>C	ENSP00000349811.3:n.841-1613T>C
ENST00000536438.5:c.841-1613T>C	ENSP00000444810.1:n.841-1613T>C
ENST00000539068.5:c.841-1613T>C	ENSP00000441205.1:n.841-1613T>C
ENST00000542713.1:c.*5142T>C	ENSP00000442340.1:n.*5142T>C
NM_001145775.2:c.841-1613T>C	NP_001139247.1:n.841-1613T>C
NM_001145776.1:c.841-1613T>C	NP_001139248.1:n.841-1613T>C
NM_001145777.1:c.*5142T>C	NP_001139249.1:n.*5142T>C
NM_004117.3:c.841-1613T>C	NP_004108.1:n.841-1613T>C
XR_242006.2:n.433-11196A>G
XR_242006.3:n.462-11196A>G
NM_001145775.3:c.841-1613T>C	NP_001139247.1:n.841-1613T>C
NM_001145776.2:c.841-1613T>C	NP_001139248.1:n.841-1613T>C
NM_001145777.2:c.*5142T>C	NP_001139249.1:n.*5142T>C
NM_004117.4:c.841-1613T>C MANE Select	NP_004108.1:n.841-1613T>C