Canonical Allele Identifier: CA1255168223

Gene: PEX13

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61032032A= , CM000664.2:g.61032032A=	GRCh38
NC_000002.11:g.61259167A= , CM000664.1:g.61259167A=	GRCh37
NC_000002.10:g.61112671A=	NCBI36
NG_008665.1:g.19356A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295030.6:c.706A= MANE Select	ENSP00000295030.4:p.Ile236=
ENST00000295030.5:c.706A=	ENSP00000295030.4:p.Ile236=
NM_002618.3:c.706A=	NP_002609.1:p.Ile236=
XM_011532904.1:c.589A=	XP_011531206.1:p.Ile197=
NM_002618.4:c.706A= MANE Select	NP_002609.1:p.Ile236=