Canonical Allele Identifier: CA1968698286

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910368G= , CM000673.2:g.45910368G=	GRCh38
NC_000011.9:g.45931919G= , CM000673.1:g.45931919G=	GRCh37
NC_000011.8:g.45888495G=	NCBI36
NG_008460.1:g.12756C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-56C= MANE Select	ENSP00000368024.5:n.953-56C=
ENST00000241041.7:c.953-191C=	ENSP00000241041.3:n.953-191C=
ENST00000378750.9:c.953-56C=	ENSP00000368024.5:n.953-56C=
ENST00000523721.2:n.183-56C=
ENST00000532681.5:c.668-56C=	ENSP00000434654.1:n.668-56C=
NM_004813.2:c.953-56C=	NP_004804.1:n.953-56C=
NM_057174.2:c.953-191C=	NP_476515.1:n.953-191C=
XM_011520474.1:c.830-56C=	XP_011518776.1:n.830-56C=
NM_004813.3:c.953-56C=	NP_004804.1:n.953-56C=
NM_004813.4:c.953-56C= MANE Select	NP_004804.2:n.953-56C=
NM_057174.3:c.953-191C=	NP_476515.2:n.953-191C=