Canonical Allele Identifier: CA1725937899

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92510996T= , CM000669.2:g.92510996T=	GRCh38
NC_000007.13:g.92140310T= , CM000669.1:g.92140310T=	GRCh37
NC_000007.12:g.91978246T=	NCBI36
NG_008341.1:g.22536A=
NG_008341.2:g.22536A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1535A= MANE Select	ENSP00000248633.4:p.Asp512=
ENST00000248633.8:c.1535A=	ENSP00000248633.4:p.Asp512=
ENST00000422866.1:c.436A=
ENST00000428214.5:c.1535A=	ENSP00000394413.1:p.Asp512=
ENST00000438045.5:c.569A=	ENSP00000410438.1:p.Asp190=
ENST00000476923.1:n.296A=
ENST00000484913.5:n.1574A=
NM_000466.2:c.1535A=	NP_000457.1:p.Asp512=
NM_001282677.1:c.1535A=	NP_001269606.1:p.Asp512=
NM_001282678.1:c.911A=	NP_001269607.1:p.Asp304=
XM_005250433.3:c.-132A=	XP_005250490.1:n.-132A=
XR_242246.3:n.1631A=
XM_017012319.2:c.-132A=	XP_016867808.1:n.-132A=
XR_001744808.2:n.645A=
XR_242246.5:n.1582A=
NM_000466.3:c.1535A= MANE Select	NP_000457.1:p.Asp512=
NM_001282677.2:c.1535A=	NP_001269606.1:p.Asp512=
NM_001282678.2:c.911A=	NP_001269607.1:p.Asp304=