Canonical Allele Identifier: CA1255168224

Gene: PEX13

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61032037C= , CM000664.2:g.61032037C=	GRCh38
NC_000002.11:g.61259172C= , CM000664.1:g.61259172C=	GRCh37
NC_000002.10:g.61112676C=	NCBI36
NG_008665.1:g.19361C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295030.6:c.711C= MANE Select	ENSP00000295030.4:p.Phe237=
ENST00000295030.5:c.711C=	ENSP00000295030.4:p.Phe237=
NM_002618.3:c.711C=	NP_002609.1:p.Phe237=
XM_011532904.1:c.594C=	XP_011531206.1:p.Phe198=
NM_002618.4:c.711C= MANE Select	NP_002609.1:p.Phe237=