Canonical Allele Identifier: CA1725947920

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517810A= , CM000669.2:g.92517810A=	GRCh38
NC_000007.13:g.92147124A= , CM000669.1:g.92147124A=	GRCh37
NC_000007.12:g.91985060A=	NCBI36
NG_008341.1:g.15722T=
NG_008341.2:g.15722T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.705T= MANE Select	ENSP00000248633.4:p.Ile235=
ENST00000248633.8:c.705T=	ENSP00000248633.4:p.Ile235=
ENST00000428214.5:c.705T=	ENSP00000394413.1:p.Ile235=
ENST00000438045.5:c.274-3843T=	ENSP00000410438.1:n.274-3843T=
ENST00000484913.5:n.744T=
NM_000466.2:c.705T=	NP_000457.1:p.Ile235=
NM_001282677.1:c.705T=	NP_001269606.1:p.Ile235=
NM_001282678.1:c.81T=	NP_001269607.1:p.Ile27=
XR_242246.3:n.801T=
XR_242246.5:n.752T=
NM_000466.3:c.705T= MANE Select	NP_000457.1:p.Ile235=
NM_001282677.2:c.705T=	NP_001269606.1:p.Ile235=
NM_001282678.2:c.81T=	NP_001269607.1:p.Ile27=