Canonical Allele Identifier: CA1725937852

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92510972G= , CM000669.2:g.92510972G=	GRCh38
NC_000007.13:g.92140286G= , CM000669.1:g.92140286G=	GRCh37
NC_000007.12:g.91978222G=	NCBI36
NG_008341.1:g.22560C=
NG_008341.2:g.22560C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1559C= MANE Select	ENSP00000248633.4:p.Pro520=
ENST00000248633.8:c.1559C=	ENSP00000248633.4:p.Pro520=
ENST00000422866.1:c.460C=
ENST00000428214.5:c.1559C=	ENSP00000394413.1:p.Pro520=
ENST00000438045.5:c.593C=	ENSP00000410438.1:p.Pro198=
ENST00000476923.1:n.320C=
ENST00000484913.5:n.1598C=
NM_000466.2:c.1559C=	NP_000457.1:p.Pro520=
NM_001282677.1:c.1559C=	NP_001269606.1:p.Pro520=
NM_001282678.1:c.935C=	NP_001269607.1:p.Pro312=
XM_005250433.3:c.-108C=	XP_005250490.1:n.-108C=
XR_242246.3:n.1655C=
XM_017012319.2:c.-108C=	XP_016867808.1:n.-108C=
XR_001744808.2:n.669C=
XR_242246.5:n.1606C=
NM_000466.3:c.1559C= MANE Select	NP_000457.1:p.Pro520=
NM_001282677.2:c.1559C=	NP_001269606.1:p.Pro520=
NM_001282678.2:c.935C=	NP_001269607.1:p.Pro312=