Canonical Allele Identifier: CA1725944799

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92509228C= , CM000669.2:g.92509228C=	GRCh38
NC_000007.13:g.92138542C= , CM000669.1:g.92138542C=	GRCh37
NC_000007.12:g.91976478C=	NCBI36
NG_008341.1:g.24304G=
NG_008341.2:g.24304G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1670+101G= MANE Select	ENSP00000248633.4:n.1670+101G=
ENST00000248633.8:c.1670+101G=	ENSP00000248633.4:n.1670+101G=
ENST00000422866.1:c.488+1716G=
ENST00000428214.5:c.1670+101G=	ENSP00000394413.1:n.1670+101G=
ENST00000438045.5:c.704+101G=	ENSP00000410438.1:n.704+101G=
ENST00000484913.5:n.1709+101G=
NM_000466.2:c.1670+101G=	NP_000457.1:n.1670+101G=
NM_001282677.1:c.1670+101G=	NP_001269606.1:n.1670+101G=
NM_001282678.1:c.1046+101G=	NP_001269607.1:n.1046+101G=
XM_005250433.3:c.-80+1716G=	XP_005250490.1:n.-80+1716G=
XR_242246.3:n.1766+101G=
XM_017012319.2:c.-80+1716G=	XP_016867808.1:n.-80+1716G=
XR_001744808.2:n.697+1716G=
XR_242246.5:n.1717+101G=
NM_000466.3:c.1670+101G= MANE Select	NP_000457.1:n.1670+101G=
NM_001282677.2:c.1670+101G=	NP_001269606.1:n.1670+101G=
NM_001282678.2:c.1046+101G=	NP_001269607.1:n.1046+101G=