Canonical Allele Identifier: CA1149571837

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408590_2408594delinsCTCAG , CM000663.2:g.2408590_2408594delinsCTCAG	GRCh38
NC_000001.10:g.2340029_2340033delinsCTCAG , CM000663.1:g.2340029_2340033delinsCTCAG	GRCh37
NC_000001.9:g.2329889_2329893delinsCTCAG	NCBI36
NG_008342.1:g.8978_8982delinsCTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.458_462delinsCTGAG	ENSP00000288774.3:p.Thr153=
ENST00000447513.7:c.458_462delinsCTGAG MANE Select	ENSP00000407922.2:p.Thr153=
ENST00000650293.1:c.412_416delinsCTGAG
ENST00000288774.7:c.458_462delinsCTGAG	ENSP00000288774.3:p.Thr153=
ENST00000447513.6:c.458_462delinsCTGAG	ENSP00000407922.2:p.Thr153=
ENST00000507596.5:c.458_462delinsCTGAG	ENSP00000424291.1:p.Thr153=
ENST00000508384.5:c.26_30delinsCTGAG	ENSP00000464289.1:p.Thr9=
ENST00000510434.1:c.458_462delinsCTGAG	ENSP00000423051.1:p.Thr153=
ENST00000515760.1:n.592_596delinsCTGAG
NM_002617.3:c.458_462delinsCTGAG	NP_002608.1:p.Thr153=
NM_153818.1:c.458_462delinsCTGAG	NP_722540.1:p.Thr153=
XM_011541573.1:c.458_462delinsCTGAG	XP_011539875.1:p.Thr153=
XM_011541574.1:c.26_30delinsCTGAG	XP_011539876.1:p.Thr9=
XM_011541575.1:c.26_30delinsCTGAG	XP_011539877.1:p.Thr9=
XM_011541576.1:c.458_462delinsCTGAG	XP_011539878.1:p.Thr153=
XR_946666.1:n.578_582delinsCTGAG
XM_011541576.2:c.458_462delinsCTGAG	XP_011539878.1:p.Thr153=
XR_946666.2:n.527_531delinsCTGAG
NM_001374425.1:c.458_462delinsCTGAG	NP_001361354.1:p.Thr153=
NM_001374426.1:c.26_30delinsCTGAG	NP_001361355.1:p.Thr9=
NM_001374427.1:c.26_30delinsCTGAG	NP_001361356.1:p.Thr9=
NM_002617.4:c.458_462delinsCTGAG MANE Select	NP_002608.1:p.Thr153=
NM_153818.2:c.458_462delinsCTGAG	NP_722540.1:p.Thr153=
NR_164636.1:n.577_581delinsCTGAG