Canonical Allele Identifier: CA1968698234

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910259C= , CM000673.2:g.45910259C=	GRCh38
NC_000011.9:g.45931810C= , CM000673.1:g.45931810C=	GRCh37
NC_000011.8:g.45888386C=	NCBI36
NG_008460.1:g.12865G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.1006G= MANE Select	ENSP00000368024.5:p.Gly336=
ENST00000241041.7:c.953-82G=	ENSP00000241041.3:n.953-82G=
ENST00000378750.9:c.1006G=	ENSP00000368024.5:p.Gly336=
ENST00000523721.2:n.236G=
ENST00000532681.5:c.721G=	ENSP00000434654.1:p.Gly241=
NM_004813.2:c.1006G=	NP_004804.1:p.Gly336=
NM_057174.2:c.953-82G=	NP_476515.1:n.953-82G=
XM_011520474.1:c.883G=	XP_011518776.1:p.Gly295=
NM_004813.3:c.1006G=	NP_004804.1:p.Gly336=
NM_004813.4:c.1006G= MANE Select	NP_004804.2:p.Gly336=
NM_057174.3:c.953-82G=	NP_476515.2:n.953-82G=