Canonical Allele Identifier: CA1725947176

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517346C= , CM000669.2:g.92517346C=	GRCh38
NC_000007.13:g.92146660C= , CM000669.1:g.92146660C=	GRCh37
NC_000007.12:g.91984596C=	NCBI36
NG_008341.1:g.16186G=
NG_008341.2:g.16186G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1169G= MANE Select	ENSP00000248633.4:p.Gly390=
ENST00000248633.8:c.1169G=	ENSP00000248633.4:p.Gly390=
ENST00000422866.1:c.70G=
ENST00000428214.5:c.1169G=	ENSP00000394413.1:p.Gly390=
ENST00000438045.5:c.274-3379G=	ENSP00000410438.1:n.274-3379G=
ENST00000484913.5:n.1208G=
NM_000466.2:c.1169G=	NP_000457.1:p.Gly390=
NM_001282677.1:c.1169G=	NP_001269606.1:p.Gly390=
NM_001282678.1:c.545G=	NP_001269607.1:p.Gly182=
XR_242246.3:n.1265G=
XM_017012319.2:c.-498G=	XP_016867808.1:n.-498G=
XR_001744808.2:n.279G=
XR_242246.5:n.1216G=
NM_000466.3:c.1169G= MANE Select	NP_000457.1:p.Gly390=
NM_001282677.2:c.1169G=	NP_001269606.1:p.Gly390=
NM_001282678.2:c.545G=	NP_001269607.1:p.Gly182=