Canonical Allele Identifier: CA566622442

Gene: FKBP5

Linked Data

• dbSNP Id: rs1468497690
• gnomAD v2: 6-35607202-A-T
• gnomAD v3: 6-35639425-A-T
• gnomAD v4: 6-35639425-A-T
• MyVariant Identifiers: chr6:g.35607202A>T (hg19) ; chr6:g.35639425A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35639425A>T , CM000668.2:g.35639425A>T	GRCh38
NC_000006.11:g.35607202A>T , CM000668.1:g.35607202A>T	GRCh37
NC_000006.10:g.35715180A>T	NCBI36
NG_012645.2:g.94159T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.106-2267T>A MANE Select	ENSP00000349811.3:n.106-2267T>A
ENST00000357266.8:c.106-2267T>A	ENSP00000349811.3:n.106-2267T>A
ENST00000536438.5:c.106-2267T>A	ENSP00000444810.1:n.106-2267T>A
ENST00000539068.5:c.106-2267T>A	ENSP00000441205.1:n.106-2267T>A
ENST00000542713.1:c.106-2267T>A	ENSP00000442340.1:n.106-2267T>A
NM_001145775.2:c.106-2267T>A	NP_001139247.1:n.106-2267T>A
NM_001145776.1:c.106-2267T>A	NP_001139248.1:n.106-2267T>A
NM_001145777.1:c.106-2267T>A	NP_001139249.1:n.106-2267T>A
NM_004117.3:c.106-2267T>A	NP_004108.1:n.106-2267T>A
XR_926743.1:n.287+5605A>T
XR_002956345.1:n.1483-9925A>T
NM_001145775.3:c.106-2267T>A	NP_001139247.1:n.106-2267T>A
NM_001145776.2:c.106-2267T>A	NP_001139248.1:n.106-2267T>A
NM_001145777.2:c.106-2267T>A	NP_001139249.1:n.106-2267T>A
NM_004117.4:c.106-2267T>A MANE Select	NP_004108.1:n.106-2267T>A