Canonical Allele Identifier: CA2642734631

Gene: PEX10

Linked Data

• gnomAD v4: 1-2408785-CGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408790_2408792del , CM000663.2:g.2408790_2408792del	GRCh38
NC_000001.10:g.2340229_2340231del , CM000663.1:g.2340229_2340231del	GRCh37
NC_000001.9:g.2330089_2330091del	NCBI36
NG_008342.1:g.8784_8786del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.264_266del	ENSP00000288774.3:p.Ser89del
ENST00000447513.7:c.264_266del MANE Select	ENSP00000407922.2:p.Ser89del
ENST00000650293.1:c.218_220del
ENST00000288774.7:c.264_266del	ENSP00000288774.3:p.Ser89del
ENST00000447513.6:c.264_266del	ENSP00000407922.2:p.Ser89del
ENST00000502666.1:c.469_471del	ENSP00000461951.1:n.469_471del
ENST00000507596.5:c.264_266del	ENSP00000424291.1:p.Ser89del
ENST00000508384.5:c.-169_-167del	ENSP00000464289.1:n.-169_-167del
ENST00000510434.1:c.264_266del	ENSP00000423051.1:p.Ser89del
ENST00000514502.1:c.*281_*283del	ENSP00000425924.1:n.*281_*283del
ENST00000515760.1:n.398_400del
NM_002617.3:c.264_266del	NP_002608.1:p.Ser89del
NM_153818.1:c.264_266del	NP_722540.1:p.Ser89del
XM_011541573.1:c.264_266del	XP_011539875.1:p.Ser89del
XM_011541574.1:c.-169_-167del	XP_011539876.1:n.-169_-167del
XM_011541575.1:c.-169_-167del	XP_011539877.1:n.-169_-167del
XM_011541576.1:c.264_266del	XP_011539878.1:p.Ser89del
XR_946666.1:n.384_386del
XM_011541576.2:c.264_266del	XP_011539878.1:p.Ser89del
XR_946666.2:n.333_335del
NM_001374425.1:c.264_266del	NP_001361354.1:p.Ser89del
NM_001374426.1:c.-169_-167del	NP_001361355.1:n.-169_-167del
NM_001374427.1:c.-169_-167del	NP_001361356.1:n.-169_-167del
NM_002617.4:c.264_266del MANE Select	NP_002608.1:p.Ser89del
NM_153818.2:c.264_266del	NP_722540.1:p.Ser89del
NR_164636.1:n.383_385del