Canonical Allele Identifier: CA1968698259

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910309G= , CM000673.2:g.45910309G=	GRCh38
NC_000011.9:g.45931860G= , CM000673.1:g.45931860G=	GRCh37
NC_000011.8:g.45888436G=	NCBI36
NG_008460.1:g.12815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.956C= MANE Select	ENSP00000368024.5:p.Pro319=
ENST00000241041.7:c.953-132C=	ENSP00000241041.3:n.953-132C=
ENST00000378750.9:c.956C=	ENSP00000368024.5:p.Pro319=
ENST00000523721.2:n.186C=
ENST00000532681.5:c.671C=	ENSP00000434654.1:p.Pro224=
NM_004813.2:c.956C=	NP_004804.1:p.Pro319=
NM_057174.2:c.953-132C=	NP_476515.1:n.953-132C=
XM_011520474.1:c.833C=	XP_011518776.1:p.Pro278=
NM_004813.3:c.956C=	NP_004804.1:p.Pro319=
NM_004813.4:c.956C= MANE Select	NP_004804.2:p.Pro319=
NM_057174.3:c.953-132C=	NP_476515.2:n.953-132C=