Canonical Allele Identifier: CA1968698137
Gene: PEX16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910082A= , CM000673.2:g.45910082A= GRCh38
NC_000011.9:g.45931633A= , CM000673.1:g.45931633A= GRCh37
NC_000011.8:g.45888209A= NCBI36
NG_008460.1:g.13042T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*172T= MANE Select ENSP00000368024.5:n.*172T=
ENST00000241041.7:c.*7T= ENSP00000241041.3:n.*7T=
NM_004813.2:c.*172T= NP_004804.1:n.*172T=
NM_057174.2:c.*7T= NP_476515.1:n.*7T=
NM_004813.3:c.*172T= NP_004804.1:n.*172T=
NM_004813.4:c.*172T= MANE Select NP_004804.2:n.*172T=
NM_057174.3:c.*7T= NP_476515.2:n.*7T=
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