Canonical Allele Identifier: CA2773371651
Gene: PEX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485370_143485371insTG , CM000668.2:g.143485370_143485371insTG GRCh38
NC_000006.11:g.143806507_143806508insTG , CM000668.1:g.143806507_143806508insTG GRCh37
NC_000006.10:g.143848200_143848201insTG NCBI36
NG_008459.1:g.39590_39591insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.1038+122_1038+123insTG MANE Select ENSP00000356563.4:n.1038+122_1038+123insTG
ENST00000367591.4:c.1038+122_1038+123insTG ENSP00000356563.4:n.1038+122_1038+123insTG
ENST00000585848.1:n.177+122_177+123insTG
NM_003630.2:c.1038+122_1038+123insTG NP_003621.1:n.1038+122_1038+123insTG
NM_003630.3:c.1038+122_1038+123insTG MANE Select NP_003621.1:n.1038+122_1038+123insTG
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