Canonical Allele Identifier: CA2579209493
Gene: PEX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.76983207_76983208insGGATGT , CM000670.2:g.76983207_76983208insGGATGT GRCh38
NC_000008.10:g.77895443_77895444insGGATGT , CM000670.1:g.77895443_77895444insGGATGT GRCh37
NC_000008.9:g.78057998_78057999insGGATGT NCBI36
NG_008371.1:g.22081_22082insACATCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000357039.9:c.*53_*54insACATCC MANE Select ENSP00000349543.4:n.*53_*54insACATCC
ENST00000357039.8:c.*53_*54insACATCC ENSP00000349543.4:n.*53_*54insACATCC
ENST00000520103.5:c.*53_*54insACATCC ENSP00000428590.1:n.*53_*54insACATCC
ENST00000522527.5:c.*53_*54insACATCC ENSP00000428638.1:n.*53_*54insACATCC
NM_000318.2:c.*53_*54insACATCC NP_000309.1:n.*53_*54insACATCC
NM_001079867.1:c.*53_*54insACATCC NP_001073336.1:n.*53_*54insACATCC
NM_001172086.1:c.*53_*54insACATCC NP_001165557.1:n.*53_*54insACATCC
NM_001172087.1:c.*53_*54insACATCC NP_001165558.1:n.*53_*54insACATCC
NM_000318.3:c.*53_*54insACATCC MANE Select NP_000309.2:n.*53_*54insACATCC
NM_001079867.2:c.*53_*54insACATCC NP_001073336.2:n.*53_*54insACATCC
NM_001172086.2:c.*53_*54insACATCC NP_001165557.2:n.*53_*54insACATCC
NM_001172087.2:c.*53_*54insACATCC NP_001165558.2:n.*53_*54insACATCC