Canonical Allele Identifier: CA1968698121
Gene: PEX16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910055C= , CM000673.2:g.45910055C= GRCh38
NC_000011.9:g.45931606C= , CM000673.1:g.45931606C= GRCh37
NC_000011.8:g.45888182C= NCBI36
NG_008460.1:g.13069G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*199G= MANE Select ENSP00000368024.5:n.*199G=
ENST00000241041.7:c.*34G= ENSP00000241041.3:n.*34G=
NM_004813.2:c.*199G= NP_004804.1:n.*199G=
NM_057174.2:c.*34G= NP_476515.1:n.*34G=
NM_004813.3:c.*199G= NP_004804.1:n.*199G=
NM_004813.4:c.*199G= MANE Select NP_004804.2:n.*199G=
NM_057174.3:c.*34G= NP_476515.2:n.*34G=
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