Canonical Allele Identifier: CA1968698078
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45909969C= , CM000673.2:g.45909969C= GRCh38
NC_000011.9:g.45931520C= , CM000673.1:g.45931520C= GRCh37
NC_000011.8:g.45888096C= NCBI36
NG_008460.1:g.13155G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*285G= MANE Select ENSP00000368024.5:n.*285G=
ENST00000241041.7:c.*120G= ENSP00000241041.3:n.*120G=
NM_004813.2:c.*285G= NP_004804.1:n.*285G=
NM_057174.2:c.*120G= NP_476515.1:n.*120G=
NM_004813.3:c.*285G= NP_004804.1:n.*285G=
NM_004813.4:c.*285G= MANE Select NP_004804.2:n.*285G=
NM_057174.3:c.*120G= NP_476515.2:n.*120G=