Canonical Allele Identifier: CA1145310471

Gene: PEX10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2406412_2406418delinsCTGCTGC , CM000663.2:g.2406412_2406418delinsCTGCTGC	GRCh38
NC_000001.10:g.2337851_2337857delinsCTGCTGC , CM000663.1:g.2337851_2337857delinsCTGCTGC	GRCh37
NC_000001.9:g.2327711_2327717delinsCTGCTGC	NCBI36
NG_008342.1:g.11154_11160delinsGCAGCAG
NG_016128.1:g.19638_19644delinsCTGCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288774.8:c.972+66_972+72delinsGCAGCAG	ENSP00000288774.3:n.972+66_972+72delinsGCAGCAG
ENST00000447513.7:c.912+66_912+72delinsGCAGCAG MANE Select	ENSP00000407922.2:n.912+66_912+72delinsGCAGCAG
ENST00000650293.1:c.866+66_866+72delinsGCAGCAG
ENST00000288774.7:c.972+66_972+72delinsGCAGCAG	ENSP00000288774.3:n.972+66_972+72delinsGCAGCAG
ENST00000447513.6:c.912+66_912+72delinsGCAGCAG	ENSP00000407922.2:n.912+66_912+72delinsGCAGCAG
ENST00000507596.5:c.912+66_912+72delinsGCAGCAG	ENSP00000424291.1:n.912+66_912+72delinsGCAGCAG
NM_002617.3:c.912+66_912+72delinsGCAGCAG	NP_002608.1:n.912+66_912+72delinsGCAGCAG
NM_153818.1:c.972+66_972+72delinsGCAGCAG	NP_722540.1:n.972+66_972+72delinsGCAGCAG
XM_011541573.1:c.969+66_969+72delinsGCAGCAG	XP_011539875.1:n.969+66_969+72delinsGCAGCAG
XM_011541574.1:c.537+66_537+72delinsGCAGCAG	XP_011539876.1:n.537+66_537+72delinsGCAGCAG
XM_011541575.1:c.537+66_537+72delinsGCAGCAG	XP_011539877.1:n.537+66_537+72delinsGCAGCAG
XR_946666.1:n.1028+66_1028+72delinsGCAGCAG
XR_946666.2:n.977+66_977+72delinsGCAGCAG
NM_001374425.1:c.969+66_969+72delinsGCAGCAG	NP_001361354.1:n.969+66_969+72delinsGCAGCAG
NM_001374426.1:c.537+66_537+72delinsGCAGCAG	NP_001361355.1:n.537+66_537+72delinsGCAGCAG
NM_001374427.1:c.480+66_480+72delinsGCAGCAG	NP_001361356.1:n.480+66_480+72delinsGCAGCAG
NM_002617.4:c.912+66_912+72delinsGCAGCAG MANE Select	NP_002608.1:n.912+66_912+72delinsGCAGCAG
NM_153818.2:c.972+66_972+72delinsGCAGCAG	NP_722540.1:n.972+66_972+72delinsGCAGCAG
NR_164636.1:n.1027+66_1027+72delinsGCAGCAG