Canonical Allele Identifier: CA1725936110

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92501972C= , CM000669.2:g.92501972C=	GRCh38
NC_000007.13:g.92131286C= , CM000669.1:g.92131286C=	GRCh37
NC_000007.12:g.91969222C=	NCBI36
NG_008341.1:g.31560G=
NG_008341.2:g.31560G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2334G= MANE Select	ENSP00000248633.4:p.Gly778=
ENST00000248633.8:c.2334G=	ENSP00000248633.4:p.Gly778=
ENST00000428214.5:c.2163G=	ENSP00000394413.1:p.Gly721=
ENST00000438045.5:c.1368G=	ENSP00000410438.1:p.Gly456=
ENST00000484913.5:n.2373G=
ENST00000496092.1:n.132G=
ENST00000496420.5:n.2010G=
NM_000466.2:c.2334G=	NP_000457.1:p.Gly778=
NM_001282677.1:c.2163G=	NP_001269606.1:p.Gly721=
NM_001282678.1:c.1710G=	NP_001269607.1:p.Gly570=
XM_005250433.3:c.585G=	XP_005250490.1:p.Gly195=
XR_242246.3:n.2430G=
XM_017012319.2:c.585G=	XP_016867808.1:p.Gly195=
XR_001744808.2:n.1361G=
XR_242246.5:n.2381G=
NM_000466.3:c.2334G= MANE Select	NP_000457.1:p.Gly778=
NM_001282677.2:c.2163G=	NP_001269606.1:p.Gly721=
NM_001282678.2:c.1710G=	NP_001269607.1:p.Gly570=