Canonical Allele Identifier: CA1620978074

Gene: FKBP5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35611226_35611232delinsCTATTAT , CM000668.2:g.35611226_35611232delinsCTATTAT	GRCh38
NC_000006.11:g.35579003_35579009delinsCTATTAT , CM000668.1:g.35579003_35579009delinsCTATTAT	GRCh37
NC_000006.10:g.35686981_35686987delinsCTATTAT	NCBI36
NG_012645.2:g.122352_122358delinsATAATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.508+7864_508+7870delinsATAATAG MANE Select	ENSP00000349811.3:n.508+7864_508+7870delinsATAATAG
ENST00000357266.8:c.508+7864_508+7870delinsATAATAG	ENSP00000349811.3:n.508+7864_508+7870delinsATAATAG
ENST00000536438.5:c.508+7864_508+7870delinsATAATAG	ENSP00000444810.1:n.508+7864_508+7870delinsATAATAG
ENST00000539068.5:c.508+7864_508+7870delinsATAATAG	ENSP00000441205.1:n.508+7864_508+7870delinsATAATAG
ENST00000542713.1:c.508+7864_508+7870delinsATAATAG	ENSP00000442340.1:n.508+7864_508+7870delinsATAATAG
NM_001145775.2:c.508+7864_508+7870delinsATAATAG	NP_001139247.1:n.508+7864_508+7870delinsATAATAG
NM_001145776.1:c.508+7864_508+7870delinsATAATAG	NP_001139248.1:n.508+7864_508+7870delinsATAATAG
NM_001145777.1:c.508+7864_508+7870delinsATAATAG	NP_001139249.1:n.508+7864_508+7870delinsATAATAG
NM_004117.3:c.508+7864_508+7870delinsATAATAG	NP_004108.1:n.508+7864_508+7870delinsATAATAG
XR_926744.1:n.1937-3455_1937-3449delinsCTATTAT
XR_002956345.1:n.1482+8903_1482+8909delinsCTATTAT
NM_001145775.3:c.508+7864_508+7870delinsATAATAG	NP_001139247.1:n.508+7864_508+7870delinsATAATAG
NM_001145776.2:c.508+7864_508+7870delinsATAATAG	NP_001139248.1:n.508+7864_508+7870delinsATAATAG
NM_001145777.2:c.508+7864_508+7870delinsATAATAG	NP_001139249.1:n.508+7864_508+7870delinsATAATAG
NM_004117.4:c.508+7864_508+7870delinsATAATAG MANE Select	NP_004108.1:n.508+7864_508+7870delinsATAATAG