Canonical Allele Identifier: CA8566210

Gene: FKBP10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41817204G>A , CM000679.2:g.41817204G>A	GRCh38
NC_000017.10:g.39973456G>A , CM000679.1:g.39973456G>A	GRCh37
NC_000017.9:g.37226982G>A	NCBI36
NG_015860.1:g.9495G>A , LRG_12:g.9495G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021939.4:c.391+1G>A MANE Select	NP_068758.3:n.391+1G>A
ENST00000321562.9:c.391+1G>A MANE Select	ENSP00000317232.4:n.391+1G>A
NM_021939.3:c.391+1G>A , LRG_12t1:c.391+1G>A	NP_068758.3:n.391+1G>A
ENST00000321562.8:c.391+1G>A	ENSP00000317232.4:n.391+1G>A
ENST00000429461.5:c.211+1G>A	ENSP00000408232.1:n.211+1G>A
ENST00000489591.5:c.246-885G>A	ENSP00000466352.1:n.246-885G>A
ENST00000585664.5:c.211+1G>A	ENSP00000468703.1:n.211+1G>A
ENST00000585922.5:c.391+1G>A	ENSP00000466097.1:n.391+1G>A
ENST00000706683.1:c.391+1G>A	ENSP00000516497.1:n.391+1G>A
XM_011525099.1:c.391+1G>A	XP_011523401.1:n.391+1G>A
XM_011525099.3:c.391+1G>A	XP_011523401.1:n.391+1G>A
XM_011525100.1:c.119-885G>A	XP_011523402.1:n.119-885G>A
XM_011525100.2:c.119-885G>A	XP_011523402.1:n.119-885G>A