Canonical Allele Identifier: CA1725935176

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499772C= , CM000669.2:g.92499772C=	GRCh38
NC_000007.13:g.92129086C= , CM000669.1:g.92129086C=	GRCh37
NC_000007.12:g.91967022C=	NCBI36
NG_008341.1:g.33760G=
NG_008341.2:g.33760G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2650G= MANE Select	ENSP00000248633.4:p.Gly884=
ENST00000248633.8:c.2650G=	ENSP00000248633.4:p.Gly884=
ENST00000428214.5:c.2479G=	ENSP00000394413.1:p.Gly827=
ENST00000438045.5:c.1684G=	ENSP00000410438.1:p.Gly562=
ENST00000484913.5:n.2689G=
ENST00000496420.5:n.2542G=
NM_000466.2:c.2650G=	NP_000457.1:p.Gly884=
NM_001282677.1:c.2479G=	NP_001269606.1:p.Gly827=
NM_001282678.1:c.2026G=	NP_001269607.1:p.Gly676=
XM_005250433.3:c.901G=	XP_005250490.1:p.Gly301=
XR_242246.3:n.2746G=
XM_017012319.2:c.901G=	XP_016867808.1:p.Gly301=
XR_001744808.2:n.1677G=
XR_242246.5:n.2697G=
NM_000466.3:c.2650G= MANE Select	NP_000457.1:p.Gly884=
NM_001282677.2:c.2479G=	NP_001269606.1:p.Gly827=
NM_001282678.2:c.2026G=	NP_001269607.1:p.Gly676=