Canonical Allele Identifier: CA1725933316

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92496726C= , CM000669.2:g.92496726C=	GRCh38
NC_000007.13:g.92126040C= , CM000669.1:g.92126040C=	GRCh37
NC_000007.12:g.91963976C=	NCBI36
NG_008341.1:g.36806G=
NG_008341.2:g.36806G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2770G= MANE Select	ENSP00000248633.4:p.Asp924=
ENST00000248633.8:c.2770G=	ENSP00000248633.4:p.Asp924=
ENST00000428214.5:c.2599G=	ENSP00000394413.1:p.Asp867=
ENST00000438045.5:c.1804G=	ENSP00000410438.1:p.Asp602=
ENST00000484913.5:n.2809G=
ENST00000496420.5:n.2662G=
NM_000466.2:c.2770G=	NP_000457.1:p.Asp924=
NM_001282677.1:c.2599G=	NP_001269606.1:p.Asp867=
NM_001282678.1:c.2146G=	NP_001269607.1:p.Asp716=
XM_005250433.3:c.1021G=	XP_005250490.1:p.Asp341=
XR_242246.3:n.2866G=
XM_017012319.2:c.1021G=	XP_016867808.1:p.Asp341=
XR_001744808.2:n.1797G=
XR_242246.5:n.2817G=
NM_000466.3:c.2770G= MANE Select	NP_000457.1:p.Asp924=
NM_001282677.2:c.2599G=	NP_001269606.1:p.Asp867=
NM_001282678.2:c.2146G=	NP_001269607.1:p.Asp716=