Canonical Allele Identifier: CA500208388

Gene: FKBP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41818090G>C , CM000679.2:g.41818090G>C	GRCh38
NC_000017.10:g.39974342G>C , CM000679.1:g.39974342G>C	GRCh37
NC_000017.9:g.37227868G>C	NCBI36
NG_015860.1:g.10381G>C , LRG_12:g.10381G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_021939.4:c.393G>C MANE Select	NP_068758.3:p.Ala131=
ENST00000321562.9:c.393G>C MANE Select	ENSP00000317232.4:p.Ala131=
NM_021939.3:c.393G>C , LRG_12t1:c.393G>C	NP_068758.3:p.Ala131=
ENST00000321562.8:c.393G>C	ENSP00000317232.4:p.Ala131=
ENST00000429461.5:c.213G>C	ENSP00000408232.1:p.Ala71=
ENST00000489591.5:c.247G>C	ENSP00000466352.1:p.Gly83Arg
ENST00000585664.5:c.213G>C	ENSP00000468703.1:p.Ala71=
ENST00000585922.5:c.393G>C	ENSP00000466097.1:p.Ala131=
ENST00000706683.1:c.393G>C	ENSP00000516497.1:p.Ala131=
XM_011525099.1:c.393G>C	XP_011523401.1:p.Ala131=
XM_011525099.3:c.393G>C	XP_011523401.1:p.Ala131=
XM_011525100.1:c.120G>C	XP_011523402.1:p.Ala40=
XM_011525100.2:c.120G>C	XP_011523402.1:p.Ala40=