Canonical Allele Identifier: CA1725941176

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506300T= , CM000669.2:g.92506300T=	GRCh38
NC_000007.13:g.92135614T= , CM000669.1:g.92135614T=	GRCh37
NC_000007.12:g.91973550T=	NCBI36
NG_008341.1:g.27232A=
NG_008341.2:g.27232A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1848A= MANE Select	ENSP00000248633.4:p.Ala616=
ENST00000248633.8:c.1848A=	ENSP00000248633.4:p.Ala616=
ENST00000422866.1:c.666A=
ENST00000428214.5:c.1848A=	ENSP00000394413.1:p.Ala616=
ENST00000438045.5:c.882A=	ENSP00000410438.1:p.Ala294=
ENST00000484913.5:n.1887A=
ENST00000496420.5:n.1524A=
NM_000466.2:c.1848A=	NP_000457.1:p.Ala616=
NM_001282677.1:c.1848A=	NP_001269606.1:p.Ala616=
NM_001282678.1:c.1224A=	NP_001269607.1:p.Ala408=
XM_005250433.3:c.99A=	XP_005250490.1:p.Ala33=
XR_242246.3:n.1944A=
XM_017012319.2:c.99A=	XP_016867808.1:p.Ala33=
XR_001744808.2:n.875A=
XR_242246.5:n.1895A=
NM_000466.3:c.1848A= MANE Select	NP_000457.1:p.Ala616=
NM_001282677.2:c.1848A=	NP_001269606.1:p.Ala616=
NM_001282678.2:c.1224A=	NP_001269607.1:p.Ala408=