Canonical Allele Identifier: CA473860971
Community Standard Title: NM_004813.4(PEX16):c.768C>T (p.Ser256=)
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45913938G>A , CM000673.2:g.45913938G>A GRCh38
NC_000011.9:g.45935489G>A , CM000673.1:g.45935489G>A GRCh37
NC_000011.8:g.45892065G>A NCBI36
NG_008460.1:g.9186C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004813.4:c.768C>T MANE Select NP_004804.2:p.Ser256=
ENST00000378750.10:c.768C>T MANE Select ENSP00000368024.5:p.Ser256=
NM_004813.2:c.768C>T NP_004804.1:p.Ser256=
NM_004813.3:c.768C>T NP_004804.1:p.Ser256=
NM_057174.2:c.768C>T NP_476515.1:p.Ser256=
NM_057174.3:c.768C>T NP_476515.2:p.Ser256=
ENST00000241041.7:c.768C>T ENSP00000241041.3:p.Ser256=
ENST00000378750.9:c.768C>T ENSP00000368024.5:p.Ser256=
ENST00000532681.5:c.483C>T ENSP00000434654.1:p.Ser161=
ENST00000533151.5:c.456C>T ENSP00000433045.1:p.Ser152=
XM_011520474.1:c.645C>T XP_011518776.1:p.Ser215=