Canonical Allele Identifier: CA1725930919

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494242_92494244delinsGAA , CM000669.2:g.92494242_92494244delinsGAA GRCh38
NC_000007.13:g.92123556_92123558delinsGAA , CM000669.1:g.92123556_92123558delinsGAA GRCh37
NC_000007.12:g.91961492_91961494delinsGAA NCBI36
NG_008341.1:g.39288_39290delinsTTC
NG_008341.2:g.39288_39290delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3030+49_3030+51delinsTTC (PEX1) MANE Select ENSP00000248633.4:n.3030+49_3030+51delinsTTC
ENST00000248633.8:c.3030+49_3030+51delinsTTC (PEX1) ENSP00000248633.4:n.3030+49_3030+51delinsTTC
ENST00000428214.5:c.2859+49_2859+51delinsTTC (PEX1) ENSP00000394413.1:n.2859+49_2859+51delinsTTC
ENST00000438045.5:c.2064+49_2064+51delinsTTC (PEX1) ENSP00000410438.1:n.2064+49_2064+51delinsTTC
ENST00000484913.5:n.3069+49_3069+51delinsTTC (PEX1)
ENST00000496420.5:n.2971_2973delinsTTC (PEX1)
NM_000466.2:c.3030+49_3030+51delinsTTC (PEX1) NP_000457.1:n.3030+49_3030+51delinsTTC
NM_001282677.1:c.2859+49_2859+51delinsTTC (PEX1) NP_001269606.1:n.2859+49_2859+51delinsTTC
NM_001282678.1:c.2406+49_2406+51delinsTTC (PEX1) NP_001269607.1:n.2406+49_2406+51delinsTTC
XM_005250433.3:c.1281+49_1281+51delinsTTC (PEX1) XP_005250490.1:n.1281+49_1281+51delinsTTC
XR_242246.3:n.3126+49_3126+51delinsTTC (PEX1)
XM_017012319.2:c.1281+49_1281+51delinsTTC (PEX1) XP_016867808.1:n.1281+49_1281+51delinsTTC
XR_001744808.2:n.2057+49_2057+51delinsTTC (PEX1)
XR_001744843.2:n.5211_5213delinsGAA (GATAD1)
XR_242246.5:n.3077+49_3077+51delinsTTC (PEX1)
XR_927494.3:n.4062_4064delinsGAA (GATAD1)
XR_927503.3:n.3993_3995delinsGAA (GATAD1)
NM_000466.3:c.3030+49_3030+51delinsTTC (PEX1) MANE Select NP_000457.1:n.3030+49_3030+51delinsTTC
NM_001282677.2:c.2859+49_2859+51delinsTTC (PEX1) NP_001269606.1:n.2859+49_2859+51delinsTTC
NM_001282678.2:c.2406+49_2406+51delinsTTC (PEX1) NP_001269607.1:n.2406+49_2406+51delinsTTC