Canonical Allele Identifier: CA1725947419

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517502A= , CM000669.2:g.92517502A=	GRCh38
NC_000007.13:g.92146816A= , CM000669.1:g.92146816A=	GRCh37
NC_000007.12:g.91984752A=	NCBI36
NG_008341.1:g.16030T=
NG_008341.2:g.16030T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1013T= MANE Select	ENSP00000248633.4:p.Leu338=
ENST00000248633.8:c.1013T=	ENSP00000248633.4:p.Leu338=
ENST00000428214.5:c.1013T=	ENSP00000394413.1:p.Leu338=
ENST00000438045.5:c.274-3535T=	ENSP00000410438.1:n.274-3535T=
ENST00000484913.5:n.1052T=
NM_000466.2:c.1013T=	NP_000457.1:p.Leu338=
NM_001282677.1:c.1013T=	NP_001269606.1:p.Leu338=
NM_001282678.1:c.389T=	NP_001269607.1:p.Leu130=
XR_242246.3:n.1109T=
XM_017012319.2:c.-654T=	XP_016867808.1:n.-654T=
XR_001744808.2:n.123T=
XR_242246.5:n.1060T=
NM_000466.3:c.1013T= MANE Select	NP_000457.1:p.Leu338=
NM_001282677.2:c.1013T=	NP_001269606.1:p.Leu338=
NM_001282678.2:c.389T=	NP_001269607.1:p.Leu130=