Canonical Allele Identifier: CA1620978104

Gene: FKBP5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35611248_35611249delinsCT , CM000668.2:g.35611248_35611249delinsCT	GRCh38
NC_000006.11:g.35579025_35579026delinsCT , CM000668.1:g.35579025_35579026delinsCT	GRCh37
NC_000006.10:g.35687003_35687004delinsCT	NCBI36
NG_012645.2:g.122335_122336delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.508+7847_508+7848delinsAG MANE Select	ENSP00000349811.3:n.508+7847_508+7848delinsAG
ENST00000357266.8:c.508+7847_508+7848delinsAG	ENSP00000349811.3:n.508+7847_508+7848delinsAG
ENST00000536438.5:c.508+7847_508+7848delinsAG	ENSP00000444810.1:n.508+7847_508+7848delinsAG
ENST00000539068.5:c.508+7847_508+7848delinsAG	ENSP00000441205.1:n.508+7847_508+7848delinsAG
ENST00000542713.1:c.508+7847_508+7848delinsAG	ENSP00000442340.1:n.508+7847_508+7848delinsAG
NM_001145775.2:c.508+7847_508+7848delinsAG	NP_001139247.1:n.508+7847_508+7848delinsAG
NM_001145776.1:c.508+7847_508+7848delinsAG	NP_001139248.1:n.508+7847_508+7848delinsAG
NM_001145777.1:c.508+7847_508+7848delinsAG	NP_001139249.1:n.508+7847_508+7848delinsAG
NM_004117.3:c.508+7847_508+7848delinsAG	NP_004108.1:n.508+7847_508+7848delinsAG
XR_926744.1:n.1937-3433_1937-3432delinsCT
XR_002956345.1:n.1482+8925_1482+8926delinsCT
NM_001145775.3:c.508+7847_508+7848delinsAG	NP_001139247.1:n.508+7847_508+7848delinsAG
NM_001145776.2:c.508+7847_508+7848delinsAG	NP_001139248.1:n.508+7847_508+7848delinsAG
NM_001145777.2:c.508+7847_508+7848delinsAG	NP_001139249.1:n.508+7847_508+7848delinsAG
NM_004117.4:c.508+7847_508+7848delinsAG MANE Select	NP_004108.1:n.508+7847_508+7848delinsAG