Canonical Allele Identifier: CA1725933399

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496771C= , CM000669.2:g.92496771C=	GRCh38
NC_000007.13:g.92126085C= , CM000669.1:g.92126085C=	GRCh37
NC_000007.12:g.91964021C=	NCBI36
NG_008341.1:g.36761G=
NG_008341.2:g.36761G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2725G= MANE Select	ENSP00000248633.4:p.Glu909=
ENST00000248633.8:c.2725G=	ENSP00000248633.4:p.Glu909=
ENST00000428214.5:c.2554G=	ENSP00000394413.1:p.Glu852=
ENST00000438045.5:c.1759G=	ENSP00000410438.1:p.Glu587=
ENST00000484913.5:n.2764G=
ENST00000496420.5:n.2617G=
NM_000466.2:c.2725G=	NP_000457.1:p.Glu909=
NM_001282677.1:c.2554G=	NP_001269606.1:p.Glu852=
NM_001282678.1:c.2101G=	NP_001269607.1:p.Glu701=
XM_005250433.3:c.976G=	XP_005250490.1:p.Glu326=
XR_242246.3:n.2821G=
XM_017012319.2:c.976G=	XP_016867808.1:p.Glu326=
XR_001744808.2:n.1752G=
XR_242246.5:n.2772G=
NM_000466.3:c.2725G= MANE Select	NP_000457.1:p.Glu909=
NM_001282677.2:c.2554G=	NP_001269606.1:p.Glu852=
NM_001282678.2:c.2101G=	NP_001269607.1:p.Glu701=