Canonical Allele Identifier: CA1255168181

Gene: PEX13

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61031930A= , CM000664.2:g.61031930A=	GRCh38
NC_000002.11:g.61259065A= , CM000664.1:g.61259065A=	GRCh37
NC_000002.10:g.61112569A=	NCBI36
NG_008665.1:g.19254A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295030.6:c.604A= MANE Select	ENSP00000295030.4:p.Arg202=
ENST00000295030.5:c.604A=	ENSP00000295030.4:p.Arg202=
NM_002618.3:c.604A=	NP_002609.1:p.Arg202=
XM_011532904.1:c.487A=	XP_011531206.1:p.Arg163=
NM_002618.4:c.604A= MANE Select	NP_002609.1:p.Arg202=