Canonical Allele Identifier: CA2770633777

Gene: FKBP5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35611267C>T , CM000668.2:g.35611267C>T	GRCh38
NC_000006.11:g.35579044C>T , CM000668.1:g.35579044C>T	GRCh37
NC_000006.10:g.35687022C>T	NCBI36
NG_012645.2:g.122317G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357266.9:c.508+7829G>A MANE Select	ENSP00000349811.3:n.508+7829G>A
ENST00000357266.8:c.508+7829G>A	ENSP00000349811.3:n.508+7829G>A
ENST00000536438.5:c.508+7829G>A	ENSP00000444810.1:n.508+7829G>A
ENST00000539068.5:c.508+7829G>A	ENSP00000441205.1:n.508+7829G>A
ENST00000542713.1:c.508+7829G>A	ENSP00000442340.1:n.508+7829G>A
NM_001145775.2:c.508+7829G>A	NP_001139247.1:n.508+7829G>A
NM_001145776.1:c.508+7829G>A	NP_001139248.1:n.508+7829G>A
NM_001145777.1:c.508+7829G>A	NP_001139249.1:n.508+7829G>A
NM_004117.3:c.508+7829G>A	NP_004108.1:n.508+7829G>A
XR_926744.1:n.1937-3414C>T
XR_002956345.1:n.1482+8944C>T
NM_001145775.3:c.508+7829G>A	NP_001139247.1:n.508+7829G>A
NM_001145776.2:c.508+7829G>A	NP_001139248.1:n.508+7829G>A
NM_001145777.2:c.508+7829G>A	NP_001139249.1:n.508+7829G>A
NM_004117.4:c.508+7829G>A MANE Select	NP_004108.1:n.508+7829G>A