Canonical Allele Identifier: CA2260200569

Gene: FKBP10

Linked Data

• dbSNP Id: rs2047861741
• gnomAD v4: 17-41819475-TGGAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41819478_41819482del , CM000679.2:g.41819478_41819482del	GRCh38
NC_000017.10:g.39975730_39975734del , CM000679.1:g.39975730_39975734del	GRCh37
NC_000017.9:g.37229256_37229260del	NCBI36
NG_015860.1:g.11769_11773del , LRG_12:g.11769_11773del

Transcript Alleles

HGVS	Amino-acid change
ENST00000706683.1:c.728-791_728-787del	ENSP00000516497.1:n.728-791_728-787del
ENST00000321562.9:c.918-52_918-48del MANE Select	ENSP00000317232.4:n.918-52_918-48del
ENST00000321562.8:c.918-52_918-48del	ENSP00000317232.4:n.918-52_918-48del
ENST00000455106.1:c.146-52_146-48del
ENST00000487489.1:n.531-52_531-48del
ENST00000489591.5:c.*328-52_*328-48del	ENSP00000466352.1:n.*328-52_*328-48del
NM_021939.3:c.918-52_918-48del , LRG_12t1:c.918-52_918-48del	NP_068758.3:n.918-52_918-48del
XM_011525099.1:c.918-52_918-48del	XP_011523401.1:n.918-52_918-48del
XM_011525100.1:c.645-52_645-48del	XP_011523402.1:n.645-52_645-48del
XM_011525099.3:c.918-52_918-48del	XP_011523401.1:n.918-52_918-48del
XM_011525100.2:c.645-52_645-48del	XP_011523402.1:n.645-52_645-48del
NM_021939.4:c.918-52_918-48del MANE Select	NP_068758.3:n.918-52_918-48del