Canonical Allele Identifier: CA2637867407

Gene: FKBP10

Linked Data

• gnomAD v4: 17-41819484-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41819484A>G , CM000679.2:g.41819484A>G	GRCh38
NC_000017.10:g.39975736A>G , CM000679.1:g.39975736A>G	GRCh37
NC_000017.9:g.37229262A>G	NCBI36
NG_015860.1:g.11775A>G , LRG_12:g.11775A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706683.1:c.728-785A>G	ENSP00000516497.1:n.728-785A>G
ENST00000321562.9:c.918-46A>G MANE Select	ENSP00000317232.4:n.918-46A>G
ENST00000321562.8:c.918-46A>G	ENSP00000317232.4:n.918-46A>G
ENST00000455106.1:c.146-46A>G
ENST00000487489.1:n.531-46A>G
ENST00000489591.5:c.*328-46A>G	ENSP00000466352.1:n.*328-46A>G
NM_021939.3:c.918-46A>G , LRG_12t1:c.918-46A>G	NP_068758.3:n.918-46A>G
XM_011525099.1:c.918-46A>G	XP_011523401.1:n.918-46A>G
XM_011525100.1:c.645-46A>G	XP_011523402.1:n.645-46A>G
XM_011525099.3:c.918-46A>G	XP_011523401.1:n.918-46A>G
XM_011525100.2:c.645-46A>G	XP_011523402.1:n.645-46A>G
NM_021939.4:c.918-46A>G MANE Select	NP_068758.3:n.918-46A>G