Canonical Allele Identifier: CA1795350946

Gene: PEX2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76983439_76983441delinsCAT , CM000670.2:g.76983439_76983441delinsCAT	GRCh38
NC_000008.10:g.77895675_77895677delinsCAT , CM000670.1:g.77895675_77895677delinsCAT	GRCh37
NC_000008.9:g.78058230_78058232delinsCAT	NCBI36
NG_008371.1:g.21848_21850delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000357039.9:c.738_740delinsATG MANE Select	ENSP00000349543.4:p.Leu246=
ENST00000357039.8:c.738_740delinsATG	ENSP00000349543.4:p.Leu246=
ENST00000520103.5:c.738_740delinsATG	ENSP00000428590.1:p.Leu246=
ENST00000522527.5:c.738_740delinsATG	ENSP00000428638.1:p.Leu246=
NM_000318.2:c.738_740delinsATG	NP_000309.1:p.Leu246=
NM_001079867.1:c.738_740delinsATG	NP_001073336.1:p.Leu246=
NM_001172086.1:c.738_740delinsATG	NP_001165557.1:p.Leu246=
NM_001172087.1:c.738_740delinsATG	NP_001165558.1:p.Leu246=
NM_000318.3:c.738_740delinsATG MANE Select	NP_000309.2:p.Leu246=
NM_001079867.2:c.738_740delinsATG	NP_001073336.2:p.Leu246=
NM_001172086.2:c.738_740delinsATG	NP_001165557.2:p.Leu246=
NM_001172087.2:c.738_740delinsATG	NP_001165558.2:p.Leu246=