Canonical Allele Identifier: CA1725931958

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92494897C= , CM000669.2:g.92494897C=	GRCh38
NC_000007.13:g.92124211C= , CM000669.1:g.92124211C=	GRCh37
NC_000007.12:g.91962147C=	NCBI36
NG_008341.1:g.38635G=
NG_008341.2:g.38635G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2784-268G= MANE Select	ENSP00000248633.4:n.2784-268G=
ENST00000248633.8:c.2784-268G=	ENSP00000248633.4:n.2784-268G=
ENST00000428214.5:c.2613-268G=	ENSP00000394413.1:n.2613-268G=
ENST00000438045.5:c.1818-268G=	ENSP00000410438.1:n.1818-268G=
ENST00000484913.5:n.2823-268G=
ENST00000496420.5:n.2676-268G=
NM_000466.2:c.2784-268G=	NP_000457.1:n.2784-268G=
NM_001282677.1:c.2613-268G=	NP_001269606.1:n.2613-268G=
NM_001282678.1:c.2160-268G=	NP_001269607.1:n.2160-268G=
XM_005250433.3:c.1035-268G=	XP_005250490.1:n.1035-268G=
XR_242246.3:n.2880-268G=
XM_017012319.2:c.1035-268G=	XP_016867808.1:n.1035-268G=
XR_001744808.2:n.1811-268G=
XR_242246.5:n.2831-268G=
NM_000466.3:c.2784-268G= MANE Select	NP_000457.1:n.2784-268G=
NM_001282677.2:c.2613-268G=	NP_001269606.1:n.2613-268G=
NM_001282678.2:c.2160-268G=	NP_001269607.1:n.2160-268G=