Canonical Allele Identifier: CA2642719608

Gene: PEX10

Linked Data

• gnomAD v4: 1-2406417-GCAGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406421_2406424del , CM000663.2:g.2406421_2406424del	GRCh38
NC_000001.10:g.2337860_2337863del , CM000663.1:g.2337860_2337863del	GRCh37
NC_000001.9:g.2327720_2327723del	NCBI36
NG_008342.1:g.11151_11154del
NG_016128.1:g.19647_19650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.972+63_972+66del	ENSP00000288774.3:n.972+63_972+66del
ENST00000447513.7:c.912+63_912+66del MANE Select	ENSP00000407922.2:n.912+63_912+66del
ENST00000650293.1:c.866+63_866+66del
ENST00000288774.7:c.972+63_972+66del	ENSP00000288774.3:n.972+63_972+66del
ENST00000447513.6:c.912+63_912+66del	ENSP00000407922.2:n.912+63_912+66del
ENST00000507596.5:c.912+63_912+66del	ENSP00000424291.1:n.912+63_912+66del
NM_002617.3:c.912+63_912+66del	NP_002608.1:n.912+63_912+66del
NM_153818.1:c.972+63_972+66del	NP_722540.1:n.972+63_972+66del
XM_011541573.1:c.969+63_969+66del	XP_011539875.1:n.969+63_969+66del
XM_011541574.1:c.537+63_537+66del	XP_011539876.1:n.537+63_537+66del
XM_011541575.1:c.537+63_537+66del	XP_011539877.1:n.537+63_537+66del
XR_946666.1:n.1028+63_1028+66del
XR_946666.2:n.977+63_977+66del
NM_001374425.1:c.969+63_969+66del	NP_001361354.1:n.969+63_969+66del
NM_001374426.1:c.537+63_537+66del	NP_001361355.1:n.537+63_537+66del
NM_001374427.1:c.480+63_480+66del	NP_001361356.1:n.480+63_480+66del
NM_002617.4:c.912+63_912+66del MANE Select	NP_002608.1:n.912+63_912+66del
NM_153818.2:c.972+63_972+66del	NP_722540.1:n.972+63_972+66del
NR_164636.1:n.1027+63_1027+66del