Canonical Allele Identifier: CA1725930958

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494263G= , CM000669.2:g.92494263G= GRCh38
NC_000007.13:g.92123577G= , CM000669.1:g.92123577G= GRCh37
NC_000007.12:g.91961513G= NCBI36
NG_008341.1:g.39269C=
NG_008341.2:g.39269C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3030+30C= (PEX1) MANE Select ENSP00000248633.4:n.3030+30C=
ENST00000248633.8:c.3030+30C= (PEX1) ENSP00000248633.4:n.3030+30C=
ENST00000428214.5:c.2859+30C= (PEX1) ENSP00000394413.1:n.2859+30C=
ENST00000438045.5:c.2064+30C= (PEX1) ENSP00000410438.1:n.2064+30C=
ENST00000484913.5:n.3069+30C= (PEX1)
ENST00000496420.5:n.2952C= (PEX1)
NM_000466.2:c.3030+30C= (PEX1) NP_000457.1:n.3030+30C=
NM_001282677.1:c.2859+30C= (PEX1) NP_001269606.1:n.2859+30C=
NM_001282678.1:c.2406+30C= (PEX1) NP_001269607.1:n.2406+30C=
XM_005250433.3:c.1281+30C= (PEX1) XP_005250490.1:n.1281+30C=
XR_242246.3:n.3126+30C= (PEX1)
XM_017012319.2:c.1281+30C= (PEX1) XP_016867808.1:n.1281+30C=
XR_001744808.2:n.2057+30C= (PEX1)
XR_001744843.2:n.5232G= (GATAD1)
XR_242246.5:n.3077+30C= (PEX1)
XR_927494.3:n.4083G= (GATAD1)
XR_927503.3:n.4014G= (GATAD1)
NM_000466.3:c.3030+30C= (PEX1) MANE Select NP_000457.1:n.3030+30C=
NM_001282677.2:c.2859+30C= (PEX1) NP_001269606.1:n.2859+30C=
NM_001282678.2:c.2406+30C= (PEX1) NP_001269607.1:n.2406+30C=