Canonical Allele Identifier: CA1725938006

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511044A= , CM000669.2:g.92511044A=	GRCh38
NC_000007.13:g.92140358A= , CM000669.1:g.92140358A=	GRCh37
NC_000007.12:g.91978294A=	NCBI36
NG_008341.1:g.22488T=
NG_008341.2:g.22488T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1487T= MANE Select	ENSP00000248633.4:p.Leu496=
ENST00000248633.8:c.1487T=	ENSP00000248633.4:p.Leu496=
ENST00000422866.1:c.388T=
ENST00000428214.5:c.1487T=	ENSP00000394413.1:p.Leu496=
ENST00000438045.5:c.521T=	ENSP00000410438.1:p.Leu174=
ENST00000476923.1:n.248T=
ENST00000484913.5:n.1526T=
NM_000466.2:c.1487T=	NP_000457.1:p.Leu496=
NM_001282677.1:c.1487T=	NP_001269606.1:p.Leu496=
NM_001282678.1:c.863T=	NP_001269607.1:p.Leu288=
XM_005250433.3:c.-180T=	XP_005250490.1:n.-180T=
XR_242246.3:n.1583T=
XM_017012319.2:c.-180T=	XP_016867808.1:n.-180T=
XR_001744808.2:n.597T=
XR_242246.5:n.1534T=
NM_000466.3:c.1487T= MANE Select	NP_000457.1:p.Leu496=
NM_001282677.2:c.1487T=	NP_001269606.1:p.Leu496=
NM_001282678.2:c.863T=	NP_001269607.1:p.Leu288=