Canonical Allele Identifier: CA1968698213

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910227C= , CM000673.2:g.45910227C=	GRCh38
NC_000011.9:g.45931778C= , CM000673.1:g.45931778C=	GRCh37
NC_000011.8:g.45888354C=	NCBI36
NG_008460.1:g.12897G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.*27G= MANE Select	ENSP00000368024.5:n.*27G=
ENST00000241041.7:c.953-50G=	ENSP00000241041.3:n.953-50G=
ENST00000378750.9:c.*27G=	ENSP00000368024.5:n.*27G=
ENST00000523721.2:n.268G=
ENST00000532681.5:c.*27G=	ENSP00000434654.1:n.*27G=
NM_004813.2:c.*27G=	NP_004804.1:n.*27G=
NM_057174.2:c.953-50G=	NP_476515.1:n.953-50G=
XM_011520474.1:c.*27G=	XP_011518776.1:n.*27G=
NM_004813.3:c.*27G=	NP_004804.1:n.*27G=
NM_004813.4:c.*27G= MANE Select	NP_004804.2:n.*27G=
NM_057174.3:c.953-50G=	NP_476515.2:n.953-50G=