Canonical Allele Identifier: CA1725947569

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517608T= , CM000669.2:g.92517608T=	GRCh38
NC_000007.13:g.92146922T= , CM000669.1:g.92146922T=	GRCh37
NC_000007.12:g.91984858T=	NCBI36
NG_008341.1:g.15924A=
NG_008341.2:g.15924A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.907A= MANE Select	ENSP00000248633.4:p.Thr303=
ENST00000248633.8:c.907A=	ENSP00000248633.4:p.Thr303=
ENST00000428214.5:c.907A=	ENSP00000394413.1:p.Thr303=
ENST00000438045.5:c.274-3641A=	ENSP00000410438.1:n.274-3641A=
ENST00000484913.5:n.946A=
NM_000466.2:c.907A=	NP_000457.1:p.Thr303=
NM_001282677.1:c.907A=	NP_001269606.1:p.Thr303=
NM_001282678.1:c.283A=	NP_001269607.1:p.Thr95=
XR_242246.3:n.1003A=
XM_017012319.2:c.-760A=	XP_016867808.1:n.-760A=
XR_001744808.2:n.17A=
XR_242246.5:n.954A=
NM_000466.3:c.907A= MANE Select	NP_000457.1:p.Thr303=
NM_001282677.2:c.907A=	NP_001269606.1:p.Thr303=
NM_001282678.2:c.283A=	NP_001269607.1:p.Thr95=