Canonical Allele Identifier: CA2613277470
Gene: PEX16 HGNC NCBI

Linked Data

gnomAD v4: 11-45909999-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45909999G>T , CM000673.2:g.45909999G>T GRCh38
NC_000011.9:g.45931550G>T , CM000673.1:g.45931550G>T GRCh37
NC_000011.8:g.45888126G>T NCBI36
NG_008460.1:g.13125C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*255C>A MANE Select ENSP00000368024.5:n.*255C>A
ENST00000241041.7:c.*90C>A ENSP00000241041.3:n.*90C>A
NM_004813.2:c.*255C>A NP_004804.1:n.*255C>A
NM_057174.2:c.*90C>A NP_476515.1:n.*90C>A
NM_004813.3:c.*255C>A NP_004804.1:n.*255C>A
NM_004813.4:c.*255C>A MANE Select NP_004804.2:n.*255C>A
NM_057174.3:c.*90C>A NP_476515.2:n.*90C>A
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