Canonical Allele Identifier: CA1725947635

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517638G= , CM000669.2:g.92517638G=	GRCh38
NC_000007.13:g.92146952G= , CM000669.1:g.92146952G=	GRCh37
NC_000007.12:g.91984888G=	NCBI36
NG_008341.1:g.15894C=
NG_008341.2:g.15894C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.877C= MANE Select	ENSP00000248633.4:p.Gln293=
ENST00000248633.8:c.877C=	ENSP00000248633.4:p.Gln293=
ENST00000428214.5:c.877C=	ENSP00000394413.1:p.Gln293=
ENST00000438045.5:c.274-3671C=	ENSP00000410438.1:n.274-3671C=
ENST00000484913.5:n.916C=
NM_000466.2:c.877C=	NP_000457.1:p.Gln293=
NM_001282677.1:c.877C=	NP_001269606.1:p.Gln293=
NM_001282678.1:c.253C=	NP_001269607.1:p.Gln85=
XR_242246.3:n.973C=
XR_242246.5:n.924C=
NM_000466.3:c.877C= MANE Select	NP_000457.1:p.Gln293=
NM_001282677.2:c.877C=	NP_001269606.1:p.Gln293=
NM_001282678.2:c.253C=	NP_001269607.1:p.Gln85=