Canonical Allele Identifier: CA1255168184

Gene: PEX13

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61031937G= , CM000664.2:g.61031937G=	GRCh38
NC_000002.11:g.61259072G= , CM000664.1:g.61259072G=	GRCh37
NC_000002.10:g.61112576G=	NCBI36
NG_008665.1:g.19261G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295030.6:c.611G= MANE Select	ENSP00000295030.4:p.Gly204=
ENST00000295030.5:c.611G=	ENSP00000295030.4:p.Gly204=
NM_002618.3:c.611G=	NP_002609.1:p.Gly204=
XM_011532904.1:c.494G=	XP_011531206.1:p.Gly165=
NM_002618.4:c.611G= MANE Select	NP_002609.1:p.Gly204=