Canonical Allele Identifier: CA1968698173
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910145C= , CM000673.2:g.45910145C= GRCh38
NC_000011.9:g.45931696C= , CM000673.1:g.45931696C= GRCh37
NC_000011.8:g.45888272C= NCBI36
NG_008460.1:g.12979G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*109G= MANE Select ENSP00000368024.5:n.*109G=
ENST00000241041.7:c.985G= ENSP00000241041.3:p.Ala329=
NM_004813.2:c.*109G= NP_004804.1:n.*109G=
NM_057174.2:c.985G= NP_476515.1:p.Ala329=
NM_004813.3:c.*109G= NP_004804.1:n.*109G=
NM_004813.4:c.*109G= MANE Select NP_004804.2:n.*109G=
NM_057174.3:c.985G= NP_476515.2:p.Ala329=