Canonical Allele Identifier: CA1968698170
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910139G= , CM000673.2:g.45910139G= GRCh38
NC_000011.9:g.45931690G= , CM000673.1:g.45931690G= GRCh37
NC_000011.8:g.45888266G= NCBI36
NG_008460.1:g.12985C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*115C= MANE Select ENSP00000368024.5:n.*115C=
ENST00000241041.7:c.991C= ENSP00000241041.3:p.Pro331=
NM_004813.2:c.*115C= NP_004804.1:n.*115C=
NM_057174.2:c.991C= NP_476515.1:p.Pro331=
NM_004813.3:c.*115C= NP_004804.1:n.*115C=
NM_004813.4:c.*115C= MANE Select NP_004804.2:n.*115C=
NM_057174.3:c.991C= NP_476515.2:p.Pro331=