Canonical Allele Identifier: CA1255168221

Gene: PEX13

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61032028G= , CM000664.2:g.61032028G=	GRCh38
NC_000002.11:g.61259163G= , CM000664.1:g.61259163G=	GRCh37
NC_000002.10:g.61112667G=	NCBI36
NG_008665.1:g.19352G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295030.6:c.702G= MANE Select	ENSP00000295030.4:p.Trp234=
ENST00000295030.5:c.702G=	ENSP00000295030.4:p.Trp234=
NM_002618.3:c.702G=	NP_002609.1:p.Trp234=
XM_011532904.1:c.585G=	XP_011531206.1:p.Trp195=
NM_002618.4:c.702G= MANE Select	NP_002609.1:p.Trp234=