Canonical Allele Identifier: CA1669274402
Gene: PEX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485108_143485109delinsTG , CM000668.2:g.143485108_143485109delinsTG GRCh38
NC_000006.11:g.143806245_143806246delinsTG , CM000668.1:g.143806245_143806246delinsTG GRCh37
NC_000006.10:g.143847938_143847939delinsTG NCBI36
NG_008459.1:g.39328_39329delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.942-44_942-43delinsTG MANE Select ENSP00000356563.4:n.942-44_942-43delinsTG
ENST00000367591.4:c.942-44_942-43delinsTG ENSP00000356563.4:n.942-44_942-43delinsTG
ENST00000585848.1:n.37_38delinsTG
NM_003630.2:c.942-44_942-43delinsTG NP_003621.1:n.942-44_942-43delinsTG
NM_003630.3:c.942-44_942-43delinsTG MANE Select NP_003621.1:n.942-44_942-43delinsTG