Canonical Allele Identifier: CA8566187

Gene: FKBP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41817121C>T , CM000679.2:g.41817121C>T	GRCh38
NC_000017.10:g.39973373C>T , CM000679.1:g.39973373C>T	GRCh37
NC_000017.9:g.37226899C>T	NCBI36
NG_015860.1:g.9412C>T , LRG_12:g.9412C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021939.4:c.309C>T MANE Select	NP_068758.3:p.Asp103=
ENST00000321562.9:c.309C>T MANE Select	ENSP00000317232.4:p.Asp103=
NM_021939.3:c.309C>T , LRG_12t1:c.309C>T	NP_068758.3:p.Asp103=
ENST00000321562.8:c.309C>T	ENSP00000317232.4:p.Asp103=
ENST00000429461.5:c.129C>T	ENSP00000408232.1:p.Asp43=
ENST00000489591.5:c.246-968C>T	ENSP00000466352.1:n.246-968C>T
ENST00000585664.5:c.129C>T	ENSP00000468703.1:p.Asp43=
ENST00000585922.5:c.309C>T	ENSP00000466097.1:p.Asp103=
ENST00000706683.1:c.309C>T	ENSP00000516497.1:p.Asp103=
XM_011525099.1:c.309C>T	XP_011523401.1:p.Asp103=
XM_011525099.3:c.309C>T	XP_011523401.1:p.Asp103=
XM_011525100.1:c.119-968C>T	XP_011523402.1:n.119-968C>T
XM_011525100.2:c.119-968C>T	XP_011523402.1:n.119-968C>T