Canonical Allele Identifier: CA1968698194
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910183G= , CM000673.2:g.45910183G= GRCh38
NC_000011.9:g.45931734G= , CM000673.1:g.45931734G= GRCh37
NC_000011.8:g.45888310G= NCBI36
NG_008460.1:g.12941C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*71C= MANE Select ENSP00000368024.5:n.*71C=
ENST00000241041.7:c.953-6C= ENSP00000241041.3:n.953-6C=
ENST00000378750.9:c.*71C= ENSP00000368024.5:n.*71C=
ENST00000523721.2:n.312C=
NM_004813.2:c.*71C= NP_004804.1:n.*71C=
NM_057174.2:c.953-6C= NP_476515.1:n.953-6C=
XM_011520474.1:c.*71C= XP_011518776.1:n.*71C=
NM_004813.3:c.*71C= NP_004804.1:n.*71C=
NM_004813.4:c.*71C= MANE Select NP_004804.2:n.*71C=
NM_057174.3:c.953-6C= NP_476515.2:n.953-6C=