Canonical Allele Identifier: CA1725938648

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504700C= , CM000669.2:g.92504700C=	GRCh38
NC_000007.13:g.92134014C= , CM000669.1:g.92134014C=	GRCh37
NC_000007.12:g.91971950C=	NCBI36
NG_008341.1:g.28832G=
NG_008341.2:g.28832G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.2071+32G= MANE Select	ENSP00000248633.4:n.2071+32G=
ENST00000248633.8:c.2071+32G=	ENSP00000248633.4:n.2071+32G=
ENST00000428214.5:c.1901-1505G=	ENSP00000394413.1:n.1901-1505G=
ENST00000438045.5:c.1105+32G=	ENSP00000410438.1:n.1105+32G=
ENST00000484913.5:n.2110+32G=
ENST00000496420.5:n.1747+32G=
NM_000466.2:c.2071+32G=	NP_000457.1:n.2071+32G=
NM_001282677.1:c.1901-1505G=	NP_001269606.1:n.1901-1505G=
NM_001282678.1:c.1447+32G=	NP_001269607.1:n.1447+32G=
XM_005250433.3:c.322+32G=	XP_005250490.1:n.322+32G=
XR_242246.3:n.2167+32G=
XM_017012319.2:c.322+32G=	XP_016867808.1:n.322+32G=
XR_001744808.2:n.1098+32G=
XR_242246.5:n.2118+32G=
NM_000466.3:c.2071+32G= MANE Select	NP_000457.1:n.2071+32G=
NM_001282677.2:c.1901-1505G=	NP_001269606.1:n.1901-1505G=
NM_001282678.2:c.1447+32G=	NP_001269607.1:n.1447+32G=