Canonical Allele Identifier: CA1968698298
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910385A= , CM000673.2:g.45910385A= GRCh38
NC_000011.9:g.45931936A= , CM000673.1:g.45931936A= GRCh37
NC_000011.8:g.45888512A= NCBI36
NG_008460.1:g.12739T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.953-73T= MANE Select ENSP00000368024.5:n.953-73T=
ENST00000241041.7:c.953-208T= ENSP00000241041.3:n.953-208T=
ENST00000378750.9:c.953-73T= ENSP00000368024.5:n.953-73T=
ENST00000523721.2:n.183-73T=
ENST00000532681.5:c.668-73T= ENSP00000434654.1:n.668-73T=
NM_004813.2:c.953-73T= NP_004804.1:n.953-73T=
NM_057174.2:c.953-208T= NP_476515.1:n.953-208T=
XM_011520474.1:c.830-73T= XP_011518776.1:n.830-73T=
NM_004813.3:c.953-73T= NP_004804.1:n.953-73T=
NM_004813.4:c.953-73T= MANE Select NP_004804.2:n.953-73T=
NM_057174.3:c.953-208T= NP_476515.2:n.953-208T=