Canonical Allele Identifier: CA2260200573

Gene: FKBP10

Linked Data

• dbSNP Id: rs1555616610
• gnomAD v4: 17-41819482-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41819482G>T , CM000679.2:g.41819482G>T	GRCh38
NC_000017.10:g.39975734G>T , CM000679.1:g.39975734G>T	GRCh37
NC_000017.9:g.37229260G>T	NCBI36
NG_015860.1:g.11773G>T , LRG_12:g.11773G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706683.1:c.728-787G>T	ENSP00000516497.1:n.728-787G>T
ENST00000321562.9:c.918-48G>T MANE Select	ENSP00000317232.4:n.918-48G>T
ENST00000321562.8:c.918-48G>T	ENSP00000317232.4:n.918-48G>T
ENST00000455106.1:c.146-48G>T
ENST00000487489.1:n.531-48G>T
ENST00000489591.5:c.*328-48G>T	ENSP00000466352.1:n.*328-48G>T
NM_021939.3:c.918-48G>T , LRG_12t1:c.918-48G>T	NP_068758.3:n.918-48G>T
XM_011525099.1:c.918-48G>T	XP_011523401.1:n.918-48G>T
XM_011525100.1:c.645-48G>T	XP_011523402.1:n.645-48G>T
XM_011525099.3:c.918-48G>T	XP_011523401.1:n.918-48G>T
XM_011525100.2:c.645-48G>T	XP_011523402.1:n.645-48G>T
NM_021939.4:c.918-48G>T MANE Select	NP_068758.3:n.918-48G>T