Canonical Allele Identifier: CA2573131882

Gene: PEX10

Linked Data

• ClinVar Variation Id: 1440916
• ClinVar RCV Id: RCV001967792
• dbSNP Id: rs2100428583

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408579del , CM000663.2:g.2408579del	GRCh38
NC_000001.10:g.2340018del , CM000663.1:g.2340018del	GRCh37
NC_000001.9:g.2329878del	NCBI36
NG_008342.1:g.8995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.475del	ENSP00000288774.3:p.Ala159ArgfsTer?
ENST00000447513.7:c.475del MANE Select	ENSP00000407922.2:p.Ala159ArgfsTer?
ENST00000650293.1:c.429del
ENST00000288774.7:c.475del	ENSP00000288774.3:p.Ala159ArgfsTer?
ENST00000447513.6:c.475del	ENSP00000407922.2:p.Ala159ArgfsTer?
ENST00000507596.5:c.475del	ENSP00000424291.1:p.Ala159ArgfsTer?
ENST00000508384.5:c.43del	ENSP00000464289.1:p.Ala15ArgfsTer?
ENST00000510434.1:c.475del	ENSP00000423051.1:p.Ala159ArgfsTer?
NM_002617.3:c.475del	NP_002608.1:p.Ala159ArgfsTer?
NM_153818.1:c.475del	NP_722540.1:p.Ala159ArgfsTer?
XM_011541573.1:c.475del	XP_011539875.1:p.Ala159ArgfsTer?
XM_011541574.1:c.43del	XP_011539876.1:p.Ala15ArgfsTer?
XM_011541575.1:c.43del	XP_011539877.1:p.Ala15ArgfsTer?
XM_011541576.1:c.475del	XP_011539878.1:p.Ala159ArgfsTer?
XR_946666.1:n.595del
XM_011541576.2:c.475del	XP_011539878.1:p.Ala159ArgfsTer?
XR_946666.2:n.544del
NM_001374425.1:c.475del	NP_001361354.1:p.Ala159ArgfsTer?
NM_001374426.1:c.43del	NP_001361355.1:p.Ala15ArgfsTer?
NM_001374427.1:c.43del	NP_001361356.1:p.Ala15ArgfsTer?
NM_002617.4:c.475del MANE Select	NP_002608.1:p.Ala159ArgfsTer?
NM_153818.2:c.475del	NP_722540.1:p.Ala159ArgfsTer?
NR_164636.1:n.594del