Canonical Allele Identifier: CA1725939190

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504896C= , CM000669.2:g.92504896C=	GRCh38
NC_000007.13:g.92134210C= , CM000669.1:g.92134210C=	GRCh37
NC_000007.12:g.91972146C=	NCBI36
NG_008341.1:g.28636G=
NG_008341.2:g.28636G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1907G= MANE Select	ENSP00000248633.4:p.Arg636=
ENST00000248633.8:c.1907G=	ENSP00000248633.4:p.Arg636=
ENST00000422866.1:c.725G=
ENST00000428214.5:c.1900+1352G=	ENSP00000394413.1:n.1900+1352G=
ENST00000438045.5:c.941G=	ENSP00000410438.1:p.Arg314=
ENST00000484913.5:n.1946G=
ENST00000496420.5:n.1583G=
NM_000466.2:c.1907G=	NP_000457.1:p.Arg636=
NM_001282677.1:c.1900+1352G=	NP_001269606.1:n.1900+1352G=
NM_001282678.1:c.1283G=	NP_001269607.1:p.Arg428=
XM_005250433.3:c.158G=	XP_005250490.1:p.Arg53=
XR_242246.3:n.2003G=
XM_017012319.2:c.158G=	XP_016867808.1:p.Arg53=
XR_001744808.2:n.934G=
XR_242246.5:n.1954G=
NM_000466.3:c.1907G= MANE Select	NP_000457.1:p.Arg636=
NM_001282677.2:c.1900+1352G=	NP_001269606.1:n.1900+1352G=
NM_001282678.2:c.1283G=	NP_001269607.1:p.Arg428=