Canonical Allele Identifier: CA1725941162

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506291T= , CM000669.2:g.92506291T=	GRCh38
NC_000007.13:g.92135605T= , CM000669.1:g.92135605T=	GRCh37
NC_000007.12:g.91973541T=	NCBI36
NG_008341.1:g.27241A=
NG_008341.2:g.27241A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1857A= MANE Select	ENSP00000248633.4:p.Lys619=
ENST00000248633.8:c.1857A=	ENSP00000248633.4:p.Lys619=
ENST00000422866.1:c.675A=
ENST00000428214.5:c.1857A=	ENSP00000394413.1:p.Lys619=
ENST00000438045.5:c.891A=	ENSP00000410438.1:p.Lys297=
ENST00000484913.5:n.1896A=
ENST00000496420.5:n.1533A=
NM_000466.2:c.1857A=	NP_000457.1:p.Lys619=
NM_001282677.1:c.1857A=	NP_001269606.1:p.Lys619=
NM_001282678.1:c.1233A=	NP_001269607.1:p.Lys411=
XM_005250433.3:c.108A=	XP_005250490.1:p.Lys36=
XR_242246.3:n.1953A=
XM_017012319.2:c.108A=	XP_016867808.1:p.Lys36=
XR_001744808.2:n.884A=
XR_242246.5:n.1904A=
NM_000466.3:c.1857A= MANE Select	NP_000457.1:p.Lys619=
NM_001282677.2:c.1857A=	NP_001269606.1:p.Lys619=
NM_001282678.2:c.1233A=	NP_001269607.1:p.Lys411=