Canonical Allele Identifier: CA1725948928

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518581T= , CM000669.2:g.92518581T=	GRCh38
NC_000007.13:g.92147895T= , CM000669.1:g.92147895T=	GRCh37
NC_000007.12:g.91985831T=	NCBI36
NG_008341.1:g.14951A=
NG_008341.2:g.14951A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.358-326A= MANE Select	ENSP00000248633.4:n.358-326A=
ENST00000248633.8:c.358-326A=	ENSP00000248633.4:n.358-326A=
ENST00000428214.5:c.358-326A=	ENSP00000394413.1:n.358-326A=
ENST00000438045.5:c.273+3521A=	ENSP00000410438.1:n.273+3521A=
ENST00000484913.5:n.397-326A=
NM_000466.2:c.358-326A=	NP_000457.1:n.358-326A=
NM_001282677.1:c.358-326A=	NP_001269606.1:n.358-326A=
NM_001282678.1:c.-267-326A=	NP_001269607.1:n.-267-326A=
XR_242246.3:n.454-326A=
XR_242246.5:n.405-326A=
NM_000466.3:c.358-326A= MANE Select	NP_000457.1:n.358-326A=
NM_001282677.2:c.358-326A=	NP_001269606.1:n.358-326A=
NM_001282678.2:c.-267-326A=	NP_001269607.1:n.-267-326A=