Canonical Allele Identifier: CA1968698220

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910237T= , CM000673.2:g.45910237T=	GRCh38
NC_000011.9:g.45931788T= , CM000673.1:g.45931788T=	GRCh37
NC_000011.8:g.45888364T=	NCBI36
NG_008460.1:g.12887A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.*17A= MANE Select	ENSP00000368024.5:n.*17A=
ENST00000241041.7:c.953-60A=	ENSP00000241041.3:n.953-60A=
ENST00000378750.9:c.*17A=	ENSP00000368024.5:n.*17A=
ENST00000523721.2:n.258A=
ENST00000532681.5:c.*17A=	ENSP00000434654.1:n.*17A=
NM_004813.2:c.*17A=	NP_004804.1:n.*17A=
NM_057174.2:c.953-60A=	NP_476515.1:n.953-60A=
XM_011520474.1:c.*17A=	XP_011518776.1:n.*17A=
NM_004813.3:c.*17A=	NP_004804.1:n.*17A=
NM_004813.4:c.*17A= MANE Select	NP_004804.2:n.*17A=
NM_057174.3:c.953-60A=	NP_476515.2:n.953-60A=