Canonical Allele Identifier: CA1968698303

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910388C= , CM000673.2:g.45910388C=	GRCh38
NC_000011.9:g.45931939C= , CM000673.1:g.45931939C=	GRCh37
NC_000011.8:g.45888515C=	NCBI36
NG_008460.1:g.12736G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-76G= MANE Select	ENSP00000368024.5:n.953-76G=
ENST00000241041.7:c.953-211G=	ENSP00000241041.3:n.953-211G=
ENST00000378750.9:c.953-76G=	ENSP00000368024.5:n.953-76G=
ENST00000523721.2:n.183-76G=
ENST00000532681.5:c.668-76G=	ENSP00000434654.1:n.668-76G=
NM_004813.2:c.953-76G=	NP_004804.1:n.953-76G=
NM_057174.2:c.953-211G=	NP_476515.1:n.953-211G=
XM_011520474.1:c.830-76G=	XP_011518776.1:n.830-76G=
NM_004813.3:c.953-76G=	NP_004804.1:n.953-76G=
NM_004813.4:c.953-76G= MANE Select	NP_004804.2:n.953-76G=
NM_057174.3:c.953-211G=	NP_476515.2:n.953-211G=