Canonical Allele Identifier: CA2687718863
Gene: PEX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.76983548_76983553dup , CM000670.2:g.76983548_76983553dup GRCh38
NC_000008.10:g.77895784_77895789dup , CM000670.1:g.77895784_77895789dup GRCh37
NC_000008.9:g.78058339_78058344dup NCBI36
NG_008371.1:g.21736_21741dup

Transcript Alleles

HGVS Amino-acid change
ENST00000357039.9:c.626_631dup MANE Select ENSP00000349543.4:p.Leu210_Ile211insThrLe...
ENST00000357039.8:c.626_631dup ENSP00000349543.4:p.Leu210_Ile211insThrLe...
ENST00000520103.5:c.626_631dup ENSP00000428590.1:p.Leu210_Ile211insThrLe...
ENST00000522527.5:c.626_631dup ENSP00000428638.1:p.Leu210_Ile211insThrLe...
NM_000318.2:c.626_631dup NP_000309.1:p.Leu210_Ile211insThrLeu
NM_001079867.1:c.626_631dup NP_001073336.1:p.Leu210_Ile211insThrLeu
NM_001172086.1:c.626_631dup NP_001165557.1:p.Leu210_Ile211insThrLeu
NM_001172087.1:c.626_631dup NP_001165558.1:p.Leu210_Ile211insThrLeu
NM_000318.3:c.626_631dup MANE Select NP_000309.2:p.Leu210_Ile211insThrLeu
NM_001079867.2:c.626_631dup NP_001073336.2:p.Leu210_Ile211insThrLeu
NM_001172086.2:c.626_631dup NP_001165557.2:p.Leu210_Ile211insThrLeu
NM_001172087.2:c.626_631dup NP_001165558.2:p.Leu210_Ile211insThrLeu