Canonical Allele Identifier: CA1725951655

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522156C= , CM000669.2:g.92522156C=	GRCh38
NC_000007.13:g.92151470C= , CM000669.1:g.92151470C=	GRCh37
NC_000007.12:g.91989406C=	NCBI36
NG_008341.1:g.11376G=
NG_008341.2:g.11376G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.219G= MANE Select	ENSP00000248633.4:p.Val73=
ENST00000248633.8:c.219G=	ENSP00000248633.4:p.Val73=
ENST00000428214.5:c.219G=	ENSP00000394413.1:p.Val73=
ENST00000438045.5:c.219G=	ENSP00000410438.1:p.Val73=
ENST00000484913.5:n.223G=
NM_000466.2:c.219G=	NP_000457.1:p.Val73=
NM_001282677.1:c.219G=	NP_001269606.1:p.Val73=
NM_001282678.1:c.-441G=	NP_001269607.1:n.-441G=
XR_242246.3:n.315G=
XR_242246.5:n.266G=
NM_000466.3:c.219G= MANE Select	NP_000457.1:p.Val73=
NM_001282677.2:c.219G=	NP_001269606.1:p.Val73=
NM_001282678.2:c.-441G=	NP_001269607.1:n.-441G=