Canonical Allele Identifier: CA1968698217

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910234C= , CM000673.2:g.45910234C=	GRCh38
NC_000011.9:g.45931785C= , CM000673.1:g.45931785C=	GRCh37
NC_000011.8:g.45888361C=	NCBI36
NG_008460.1:g.12890G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.*20G= MANE Select	ENSP00000368024.5:n.*20G=
ENST00000241041.7:c.953-57G=	ENSP00000241041.3:n.953-57G=
ENST00000378750.9:c.*20G=	ENSP00000368024.5:n.*20G=
ENST00000523721.2:n.261G=
ENST00000532681.5:c.*20G=	ENSP00000434654.1:n.*20G=
NM_004813.2:c.*20G=	NP_004804.1:n.*20G=
NM_057174.2:c.953-57G=	NP_476515.1:n.953-57G=
XM_011520474.1:c.*20G=	XP_011518776.1:n.*20G=
NM_004813.3:c.*20G=	NP_004804.1:n.*20G=
NM_004813.4:c.*20G= MANE Select	NP_004804.2:n.*20G=
NM_057174.3:c.953-57G=	NP_476515.2:n.953-57G=