Canonical Allele Identifier: CA1669274577
Gene: PEX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485293G= , CM000668.2:g.143485293G= GRCh38
NC_000006.11:g.143806430G= , CM000668.1:g.143806430G= GRCh37
NC_000006.10:g.143848123G= NCBI36
NG_008459.1:g.39513G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.1038+45G= MANE Select ENSP00000356563.4:n.1038+45G=
ENST00000367591.4:c.1038+45G= ENSP00000356563.4:n.1038+45G=
ENST00000585848.1:n.177+45G=
NM_003630.2:c.1038+45G= NP_003621.1:n.1038+45G=
NM_003630.3:c.1038+45G= MANE Select NP_003621.1:n.1038+45G=
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