Canonical Allele Identifier: CA2742182575

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406229_2406429del , CM000663.2:g.2406229_2406429del	GRCh38
NC_000001.10:g.2337668_2337868del , CM000663.1:g.2337668_2337868del	GRCh37
NC_000001.9:g.2327528_2327728del	NCBI36
NG_008342.1:g.11149_11349del
NG_016128.1:g.19455_19655del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.972+61_972+261del	ENSP00000288774.3:n.972+61_972+261del
ENST00000447513.7:c.912+61_912+261del MANE Select	ENSP00000407922.2:n.912+61_912+261del
ENST00000650293.1:c.866+61_866+261del
ENST00000288774.7:c.972+61_972+261del	ENSP00000288774.3:n.972+61_972+261del
ENST00000447513.6:c.912+61_912+261del	ENSP00000407922.2:n.912+61_912+261del
ENST00000507596.5:c.912+61_912+261del	ENSP00000424291.1:n.912+61_912+261del
NM_002617.3:c.912+61_912+261del	NP_002608.1:n.912+61_912+261del
NM_153818.1:c.972+61_972+261del	NP_722540.1:n.972+61_972+261del
XM_011541573.1:c.969+61_969+261del	XP_011539875.1:n.969+61_969+261del
XM_011541574.1:c.537+61_537+261del	XP_011539876.1:n.537+61_537+261del
XM_011541575.1:c.537+61_537+261del	XP_011539877.1:n.537+61_537+261del
XR_946666.1:n.1028+61_1028+261del
XR_946666.2:n.977+61_977+261del
NM_001374425.1:c.969+61_969+261del	NP_001361354.1:n.969+61_969+261del
NM_001374426.1:c.537+61_537+261del	NP_001361355.1:n.537+61_537+261del
NM_001374427.1:c.480+61_480+261del	NP_001361356.1:n.480+61_480+261del
NM_002617.4:c.912+61_912+261del MANE Select	NP_002608.1:n.912+61_912+261del
NM_153818.2:c.972+61_972+261del	NP_722540.1:n.972+61_972+261del
NR_164636.1:n.1027+61_1027+261del