Canonical Allele Identifier: CA1725951641

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522108C= , CM000669.2:g.92522108C=	GRCh38
NC_000007.13:g.92151422C= , CM000669.1:g.92151422C=	GRCh37
NC_000007.12:g.91989358C=	NCBI36
NG_008341.1:g.11424G=
NG_008341.2:g.11424G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.267G= MANE Select	ENSP00000248633.4:p.Gly89=
ENST00000248633.8:c.267G=	ENSP00000248633.4:p.Gly89=
ENST00000428214.5:c.267G=	ENSP00000394413.1:p.Gly89=
ENST00000438045.5:c.267G=	ENSP00000410438.1:p.Gly89=
ENST00000484913.5:n.271G=
NM_000466.2:c.267G=	NP_000457.1:p.Gly89=
NM_001282677.1:c.267G=	NP_001269606.1:p.Gly89=
NM_001282678.1:c.-393G=	NP_001269607.1:n.-393G=
XR_242246.3:n.363G=
XR_242246.5:n.314G=
NM_000466.3:c.267G= MANE Select	NP_000457.1:p.Gly89=
NM_001282677.2:c.267G=	NP_001269606.1:p.Gly89=
NM_001282678.2:c.-393G=	NP_001269607.1:n.-393G=