Canonical Allele Identifier: CA399513531

Gene: FKBP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41813158G>T , CM000679.2:g.41813158G>T	GRCh38
NC_000017.10:g.39969410G>T , CM000679.1:g.39969410G>T	GRCh37
NC_000017.9:g.37222936G>T	NCBI36
NG_015860.1:g.5449G>T , LRG_12:g.5449G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021939.4:c.124G>T MANE Select	NP_068758.3:p.Glu42Ter
ENST00000321562.9:c.124G>T MANE Select	ENSP00000317232.4:p.Glu42Ter
NM_021939.3:c.124G>T , LRG_12t1:c.124G>T	NP_068758.3:p.Glu42Ter
ENST00000321562.8:c.124G>T	ENSP00000317232.4:p.Glu42Ter
ENST00000429461.5:c.-22-35G>T	ENSP00000408232.1:n.-22-35G>T
ENST00000489591.5:c.124G>T	ENSP00000466352.1:p.Glu42Ter
ENST00000585664.5:c.-22-35G>T	ENSP00000468703.1:n.-22-35G>T
ENST00000585922.5:c.124G>T	ENSP00000466097.1:p.Glu42Ter
ENST00000706683.1:c.124G>T	ENSP00000516497.1:p.Glu42Ter
XM_011525099.1:c.124G>T	XP_011523401.1:p.Glu42Ter
XM_011525099.3:c.124G>T	XP_011523401.1:p.Glu42Ter
XM_011525100.1:c.-4G>T	XP_011523402.1:n.-4G>T
XM_011525100.2:c.-4G>T	XP_011523402.1:n.-4G>T