Canonical Allele Identifier: CA1725936076

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92501898G= , CM000669.2:g.92501898G=	GRCh38
NC_000007.13:g.92131212G= , CM000669.1:g.92131212G=	GRCh37
NC_000007.12:g.91969148G=	NCBI36
NG_008341.1:g.31634C=
NG_008341.2:g.31634C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2408C= MANE Select	ENSP00000248633.4:p.Thr803=
ENST00000248633.8:c.2408C=	ENSP00000248633.4:p.Thr803=
ENST00000428214.5:c.2237C=	ENSP00000394413.1:p.Thr746=
ENST00000438045.5:c.1442C=	ENSP00000410438.1:p.Thr481=
ENST00000484913.5:n.2447C=
ENST00000496092.1:n.206C=
ENST00000496420.5:n.2084C=
NM_000466.2:c.2408C=	NP_000457.1:p.Thr803=
NM_001282677.1:c.2237C=	NP_001269606.1:p.Thr746=
NM_001282678.1:c.1784C=	NP_001269607.1:p.Thr595=
XM_005250433.3:c.659C=	XP_005250490.1:p.Thr220=
XR_242246.3:n.2504C=
XM_017012319.2:c.659C=	XP_016867808.1:p.Thr220=
XR_001744808.2:n.1435C=
XR_242246.5:n.2455C=
NM_000466.3:c.2408C= MANE Select	NP_000457.1:p.Thr803=
NM_001282677.2:c.2237C=	NP_001269606.1:p.Thr746=
NM_001282678.2:c.1784C=	NP_001269607.1:p.Thr595=