Canonical Allele Identifier: CA1725935174

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92499769T= , CM000669.2:g.92499769T=	GRCh38
NC_000007.13:g.92129083T= , CM000669.1:g.92129083T=	GRCh37
NC_000007.12:g.91967019T=	NCBI36
NG_008341.1:g.33763A=
NG_008341.2:g.33763A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2653A= MANE Select	ENSP00000248633.4:p.Thr885=
ENST00000248633.8:c.2653A=	ENSP00000248633.4:p.Thr885=
ENST00000428214.5:c.2482A=	ENSP00000394413.1:p.Thr828=
ENST00000438045.5:c.1687A=	ENSP00000410438.1:p.Thr563=
ENST00000484913.5:n.2692A=
ENST00000496420.5:n.2545A=
NM_000466.2:c.2653A=	NP_000457.1:p.Thr885=
NM_001282677.1:c.2482A=	NP_001269606.1:p.Thr828=
NM_001282678.1:c.2029A=	NP_001269607.1:p.Thr677=
XM_005250433.3:c.904A=	XP_005250490.1:p.Thr302=
XR_242246.3:n.2749A=
XM_017012319.2:c.904A=	XP_016867808.1:p.Thr302=
XR_001744808.2:n.1680A=
XR_242246.5:n.2700A=
NM_000466.3:c.2653A= MANE Select	NP_000457.1:p.Thr885=
NM_001282677.2:c.2482A=	NP_001269606.1:p.Thr828=
NM_001282678.2:c.2029A=	NP_001269607.1:p.Thr677=