Canonical Allele Identifier: CA1725947651

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517653T= , CM000669.2:g.92517653T=	GRCh38
NC_000007.13:g.92146967T= , CM000669.1:g.92146967T=	GRCh37
NC_000007.12:g.91984903T=	NCBI36
NG_008341.1:g.15879A=
NG_008341.2:g.15879A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.862A= MANE Select	ENSP00000248633.4:p.Arg288=
ENST00000248633.8:c.862A=	ENSP00000248633.4:p.Arg288=
ENST00000428214.5:c.862A=	ENSP00000394413.1:p.Arg288=
ENST00000438045.5:c.274-3686A=	ENSP00000410438.1:n.274-3686A=
ENST00000484913.5:n.901A=
NM_000466.2:c.862A=	NP_000457.1:p.Arg288=
NM_001282677.1:c.862A=	NP_001269606.1:p.Arg288=
NM_001282678.1:c.238A=	NP_001269607.1:p.Arg80=
XR_242246.3:n.958A=
XR_242246.5:n.909A=
NM_000466.3:c.862A= MANE Select	NP_000457.1:p.Arg288=
NM_001282677.2:c.862A=	NP_001269606.1:p.Arg288=
NM_001282678.2:c.238A=	NP_001269607.1:p.Arg80=