Canonical Allele Identifier: CA2776945894

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494062_92494066del , CM000669.2:g.92494062_92494066del GRCh38
NC_000007.13:g.92123376_92123380del , CM000669.1:g.92123376_92123380del GRCh37
NC_000007.12:g.91961312_91961316del NCBI36
NG_008341.1:g.39466_39470del
NG_008341.2:g.39466_39470del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3030+227_3030+231del (PEX1) MANE Select ENSP00000248633.4:n.3030+227_3030+231del
ENST00000248633.8:c.3030+227_3030+231del (PEX1) ENSP00000248633.4:n.3030+227_3030+231del
ENST00000428214.5:c.2859+227_2859+231del (PEX1) ENSP00000394413.1:n.2859+227_2859+231del
ENST00000438045.5:c.2064+227_2064+231del (PEX1) ENSP00000410438.1:n.2064+227_2064+231del
ENST00000484913.5:n.3069+227_3069+231del (PEX1)
ENST00000496420.5:n.3149_3153del (PEX1)
NM_000466.2:c.3030+227_3030+231del (PEX1) NP_000457.1:n.3030+227_3030+231del
NM_001282677.1:c.2859+227_2859+231del (PEX1) NP_001269606.1:n.2859+227_2859+231del
NM_001282678.1:c.2406+227_2406+231del (PEX1) NP_001269607.1:n.2406+227_2406+231del
XM_005250433.3:c.1281+227_1281+231del (PEX1) XP_005250490.1:n.1281+227_1281+231del
XR_242246.3:n.3126+227_3126+231del (PEX1)
XM_017012319.2:c.1281+227_1281+231del (PEX1) XP_016867808.1:n.1281+227_1281+231del
XR_001744808.2:n.2057+227_2057+231del (PEX1)
XR_001744843.2:n.5031_5035del (GATAD1)
XR_242246.5:n.3077+227_3077+231del (PEX1)
XR_927494.3:n.3882_3886del (GATAD1)
XR_927503.3:n.3813_3817del (GATAD1)
NM_000466.3:c.3030+227_3030+231del (PEX1) MANE Select NP_000457.1:n.3030+227_3030+231del
NM_001282677.2:c.2859+227_2859+231del (PEX1) NP_001269606.1:n.2859+227_2859+231del
NM_001282678.2:c.2406+227_2406+231del (PEX1) NP_001269607.1:n.2406+227_2406+231del