Canonical Allele Identifier: CA2742182926

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2408615_2408616insACT , CM000663.2:g.2408615_2408616insACT	GRCh38
NC_000001.10:g.2340054_2340055insACT , CM000663.1:g.2340054_2340055insACT	GRCh37
NC_000001.9:g.2329914_2329915insACT	NCBI36
NG_008342.1:g.8956_8957insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.436_437insAGT	ENSP00000288774.3:p.Arg146delinsGlnCys
ENST00000447513.7:c.436_437insAGT MANE Select	ENSP00000407922.2:p.Arg146delinsGlnCys
ENST00000650293.1:c.390_391insAGT
ENST00000288774.7:c.436_437insAGT	ENSP00000288774.3:p.Arg146delinsGlnCys
ENST00000447513.6:c.436_437insAGT	ENSP00000407922.2:p.Arg146delinsGlnCys
ENST00000502666.1:c.641_642insAGT	ENSP00000461951.1:n.641_642insAGT
ENST00000507596.5:c.436_437insAGT	ENSP00000424291.1:p.Arg146delinsGlnCys
ENST00000508384.5:c.4_5insAGT	ENSP00000464289.1:p.Arg2delinsGlnCys
ENST00000510434.1:c.436_437insAGT	ENSP00000423051.1:p.Arg146delinsGlnCys
ENST00000515760.1:n.570_571insAGT
NM_002617.3:c.436_437insAGT	NP_002608.1:p.Arg146delinsGlnCys
NM_153818.1:c.436_437insAGT	NP_722540.1:p.Arg146delinsGlnCys
XM_011541573.1:c.436_437insAGT	XP_011539875.1:p.Arg146delinsGlnCys
XM_011541574.1:c.4_5insAGT	XP_011539876.1:p.Arg2delinsGlnCys
XM_011541575.1:c.4_5insAGT	XP_011539877.1:p.Arg2delinsGlnCys
XM_011541576.1:c.436_437insAGT	XP_011539878.1:p.Arg146delinsGlnCys
XR_946666.1:n.556_557insAGT
XM_011541576.2:c.436_437insAGT	XP_011539878.1:p.Arg146delinsGlnCys
XR_946666.2:n.505_506insAGT
NM_001374425.1:c.436_437insAGT	NP_001361354.1:p.Arg146delinsGlnCys
NM_001374426.1:c.4_5insAGT	NP_001361355.1:p.Arg2delinsGlnCys
NM_001374427.1:c.4_5insAGT	NP_001361356.1:p.Arg2delinsGlnCys
NM_002617.4:c.436_437insAGT MANE Select	NP_002608.1:p.Arg146delinsGlnCys
NM_153818.2:c.436_437insAGT	NP_722540.1:p.Arg146delinsGlnCys
NR_164636.1:n.555_556insAGT