Canonical Allele Identifier: CA2840505144

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408514dup , CM000663.2:g.2408514dup	GRCh38
NC_000001.10:g.2339953dup , CM000663.1:g.2339953dup	GRCh37
NC_000001.9:g.2329813dup	NCBI36
NG_008342.1:g.9058dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.538dup	ENSP00000288774.3:p.Ala180GlyfsTer?
ENST00000447513.7:c.538dup MANE Select	ENSP00000407922.2:p.Ala180GlyfsTer?
ENST00000650293.1:c.492dup
ENST00000288774.7:c.538dup	ENSP00000288774.3:p.Ala180GlyfsTer?
ENST00000447513.6:c.538dup	ENSP00000407922.2:p.Ala180GlyfsTer?
ENST00000507596.5:c.538dup	ENSP00000424291.1:p.Ala180GlyfsTer?
ENST00000510434.1:c.538dup	ENSP00000423051.1:p.Ala180GlyfsTer?
NM_002617.3:c.538dup	NP_002608.1:p.Ala180GlyfsTer?
NM_153818.1:c.538dup	NP_722540.1:p.Ala180GlyfsTer?
XM_011541573.1:c.538dup	XP_011539875.1:p.Ala180GlyfsTer?
XM_011541574.1:c.106dup	XP_011539876.1:p.Ala36GlyfsTer?
XM_011541575.1:c.106dup	XP_011539877.1:p.Ala36GlyfsTer?
XM_011541576.1:c.538dup	XP_011539878.1:p.Ala180GlyfsTer?
XR_946666.1:n.658dup
XM_011541576.2:c.538dup	XP_011539878.1:p.Ala180GlyfsTer?
XR_946666.2:n.607dup
NM_001374425.1:c.538dup	NP_001361354.1:p.Ala180GlyfsTer?
NM_001374426.1:c.106dup	NP_001361355.1:p.Ala36GlyfsTer?
NM_001374427.1:c.106dup	NP_001361356.1:p.Ala36GlyfsTer?
NM_002617.4:c.538dup MANE Select	NP_002608.1:p.Ala180GlyfsTer?
NM_153818.2:c.538dup	NP_722540.1:p.Ala180GlyfsTer?
NR_164636.1:n.657dup