Canonical Allele Identifier: CA380222803
Gene: PEX16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.45931677G>T (hg19) chr11:g.45910126G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910126G>T , CM000673.2:g.45910126G>T GRCh38
NC_000011.9:g.45931677G>T , CM000673.1:g.45931677G>T GRCh37
NC_000011.8:g.45888253G>T NCBI36
NG_008460.1:g.12998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*128C>A MANE Select ENSP00000368024.5:n.*128C>A
ENST00000241041.7:c.1004C>A ENSP00000241041.3:p.Pro335His
NM_004813.2:c.*128C>A NP_004804.1:n.*128C>A
NM_057174.2:c.1004C>A NP_476515.1:p.Pro335His
NM_004813.3:c.*128C>A NP_004804.1:n.*128C>A
NM_004813.4:c.*128C>A MANE Select NP_004804.2:n.*128C>A
NM_057174.3:c.1004C>A NP_476515.2:p.Pro335His
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