Canonical Allele Identifier: CA1968698186
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910168C= , CM000673.2:g.45910168C= GRCh38
NC_000011.9:g.45931719C= , CM000673.1:g.45931719C= GRCh37
NC_000011.8:g.45888295C= NCBI36
NG_008460.1:g.12956G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*86G= MANE Select ENSP00000368024.5:n.*86G=
ENST00000241041.7:c.962G= ENSP00000241041.3:p.Arg321=
NM_004813.2:c.*86G= NP_004804.1:n.*86G=
NM_057174.2:c.962G= NP_476515.1:p.Arg321=
NM_004813.3:c.*86G= NP_004804.1:n.*86G=
NM_004813.4:c.*86G= MANE Select NP_004804.2:n.*86G=
NM_057174.3:c.962G= NP_476515.2:p.Arg321=