Canonical Allele Identifier: CA1725938900

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504811A= , CM000669.2:g.92504811A=	GRCh38
NC_000007.13:g.92134125A= , CM000669.1:g.92134125A=	GRCh37
NC_000007.12:g.91972061A=	NCBI36
NG_008341.1:g.28721T=
NG_008341.2:g.28721T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1992T= MANE Select	ENSP00000248633.4:p.Leu664=
ENST00000248633.8:c.1992T=	ENSP00000248633.4:p.Leu664=
ENST00000428214.5:c.1900+1437T=	ENSP00000394413.1:n.1900+1437T=
ENST00000438045.5:c.1026T=	ENSP00000410438.1:p.Leu342=
ENST00000484913.5:n.2031T=
ENST00000496420.5:n.1668T=
NM_000466.2:c.1992T=	NP_000457.1:p.Leu664=
NM_001282677.1:c.1900+1437T=	NP_001269606.1:n.1900+1437T=
NM_001282678.1:c.1368T=	NP_001269607.1:p.Leu456=
XM_005250433.3:c.243T=	XP_005250490.1:p.Leu81=
XR_242246.3:n.2088T=
XM_017012319.2:c.243T=	XP_016867808.1:p.Leu81=
XR_001744808.2:n.1019T=
XR_242246.5:n.2039T=
NM_000466.3:c.1992T= MANE Select	NP_000457.1:p.Leu664=
NM_001282677.2:c.1900+1437T=	NP_001269606.1:n.1900+1437T=
NM_001282678.2:c.1368T=	NP_001269607.1:p.Leu456=