Canonical Allele Identifier: CA1725947472

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517538G= , CM000669.2:g.92517538G=	GRCh38
NC_000007.13:g.92146852G= , CM000669.1:g.92146852G=	GRCh37
NC_000007.12:g.91984788G=	NCBI36
NG_008341.1:g.15994C=
NG_008341.2:g.15994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.977C= MANE Select	ENSP00000248633.4:p.Pro326=
ENST00000248633.8:c.977C=	ENSP00000248633.4:p.Pro326=
ENST00000428214.5:c.977C=	ENSP00000394413.1:p.Pro326=
ENST00000438045.5:c.274-3571C=	ENSP00000410438.1:n.274-3571C=
ENST00000484913.5:n.1016C=
NM_000466.2:c.977C=	NP_000457.1:p.Pro326=
NM_001282677.1:c.977C=	NP_001269606.1:p.Pro326=
NM_001282678.1:c.353C=	NP_001269607.1:p.Pro118=
XR_242246.3:n.1073C=
XM_017012319.2:c.-690C=	XP_016867808.1:n.-690C=
XR_001744808.2:n.87C=
XR_242246.5:n.1024C=
NM_000466.3:c.977C= MANE Select	NP_000457.1:p.Pro326=
NM_001282677.2:c.977C=	NP_001269606.1:p.Pro326=
NM_001282678.2:c.353C=	NP_001269607.1:p.Pro118=