Canonical Allele Identifier: CA1725944925

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92509336A= , CM000669.2:g.92509336A=	GRCh38
NC_000007.13:g.92138650A= , CM000669.1:g.92138650A=	GRCh37
NC_000007.12:g.91976586A=	NCBI36
NG_008341.1:g.24196T=
NG_008341.2:g.24196T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1663T= MANE Select	ENSP00000248633.4:p.Ser555=
ENST00000248633.8:c.1663T=	ENSP00000248633.4:p.Ser555=
ENST00000422866.1:c.488+1608T=
ENST00000428214.5:c.1663T=	ENSP00000394413.1:p.Ser555=
ENST00000438045.5:c.697T=	ENSP00000410438.1:p.Ser233=
ENST00000484913.5:n.1702T=
NM_000466.2:c.1663T=	NP_000457.1:p.Ser555=
NM_001282677.1:c.1663T=	NP_001269606.1:p.Ser555=
NM_001282678.1:c.1039T=	NP_001269607.1:p.Ser347=
XM_005250433.3:c.-80+1608T=	XP_005250490.1:n.-80+1608T=
XR_242246.3:n.1759T=
XM_017012319.2:c.-80+1608T=	XP_016867808.1:n.-80+1608T=
XR_001744808.2:n.697+1608T=
XR_242246.5:n.1710T=
NM_000466.3:c.1663T= MANE Select	NP_000457.1:p.Ser555=
NM_001282677.2:c.1663T=	NP_001269606.1:p.Ser555=
NM_001282678.2:c.1039T=	NP_001269607.1:p.Ser347=