Canonical Allele Identifier: CA1620969659

Gene: FKBP5

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35599305A>C , CM000668.2:g.35599305A>C	GRCh38
NC_000006.11:g.35567082A>C , CM000668.1:g.35567082A>C	GRCh37
NC_000006.10:g.35675060A>C	NCBI36
NG_012645.2:g.134279T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.509-1901T>G MANE Select	ENSP00000349811.3:n.509-1901T>G
ENST00000357266.8:c.509-1901T>G	ENSP00000349811.3:n.509-1901T>G
ENST00000536438.5:c.509-1901T>G	ENSP00000444810.1:n.509-1901T>G
ENST00000539068.5:c.509-1901T>G	ENSP00000441205.1:n.509-1901T>G
ENST00000542713.1:c.509-1901T>G	ENSP00000442340.1:n.509-1901T>G
NM_001145775.2:c.509-1901T>G	NP_001139247.1:n.509-1901T>G
NM_001145776.1:c.509-1901T>G	NP_001139248.1:n.509-1901T>G
NM_001145777.1:c.509-1901T>G	NP_001139249.1:n.509-1901T>G
NM_004117.3:c.509-1901T>G	NP_004108.1:n.509-1901T>G
NM_001145775.3:c.509-1901T>G	NP_001139247.1:n.509-1901T>G
NM_001145776.2:c.509-1901T>G	NP_001139248.1:n.509-1901T>G
NM_001145777.2:c.509-1901T>G	NP_001139249.1:n.509-1901T>G
NM_004117.4:c.509-1901T>G MANE Select	NP_004108.1:n.509-1901T>G