Canonical Allele Identifier: CA2536154919

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494405_92494406insGGGGGAAC , CM000669.2:g.92494405_92494406insGGGGGAAC GRCh38
NC_000007.13:g.92123719_92123720insGGGGGAAC , CM000669.1:g.92123719_92123720insGGGGGAAC GRCh37
NC_000007.12:g.91961655_91961656insGGGGGAAC NCBI36
NG_008341.1:g.39126_39127insGTTCCCCC
NG_008341.2:g.39126_39127insGTTCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2927-10_2927-9insGTTCCCCC (PEX1) MANE Select ENSP00000248633.4:n.2927-10_2927-9insGTTCCCCC
ENST00000248633.8:c.2927-10_2927-9insGTTCCCCC (PEX1) ENSP00000248633.4:n.2927-10_2927-9insGTTCCCCC
ENST00000428214.5:c.2756-10_2756-9insGTTCCCCC (PEX1) ENSP00000394413.1:n.2756-10_2756-9insGTTCCCCC
ENST00000438045.5:c.1961-10_1961-9insGTTCCCCC (PEX1) ENSP00000410438.1:n.1961-10_1961-9insGTTCCCCC
ENST00000484913.5:n.2966-10_2966-9insGTTCCCCC (PEX1)
ENST00000496420.5:n.2819-10_2819-9insGTTCCCCC (PEX1)
NM_000466.2:c.2927-10_2927-9insGTTCCCCC (PEX1) NP_000457.1:n.2927-10_2927-9insGTTCCCCC
NM_001282677.1:c.2756-10_2756-9insGTTCCCCC (PEX1) NP_001269606.1:n.2756-10_2756-9insGTTCCCCC
NM_001282678.1:c.2303-10_2303-9insGTTCCCCC (PEX1) NP_001269607.1:n.2303-10_2303-9insGTTCCCCC
XM_005250433.3:c.1178-10_1178-9insGTTCCCCC (PEX1) XP_005250490.1:n.1178-10_1178-9insGTTCCCCC
XR_242246.3:n.3023-10_3023-9insGTTCCCCC (PEX1)
XM_017012319.2:c.1178-10_1178-9insGTTCCCCC (PEX1) XP_016867808.1:n.1178-10_1178-9insGTTCCCCC
XR_001744808.2:n.1954-10_1954-9insGTTCCCCC (PEX1)
XR_001744843.2:n.5374_5375insGGGGGAAC (GATAD1)
XR_242246.5:n.2974-10_2974-9insGTTCCCCC (PEX1)
XR_927494.3:n.4225_4226insGGGGGAAC (GATAD1)
XR_927503.3:n.4156_4157insGGGGGAAC (GATAD1)
NM_000466.3:c.2927-10_2927-9insGTTCCCCC (PEX1) MANE Select NP_000457.1:n.2927-10_2927-9insGTTCCCCC
NM_001282677.2:c.2756-10_2756-9insGTTCCCCC (PEX1) NP_001269606.1:n.2756-10_2756-9insGTTCCCCC
NM_001282678.2:c.2303-10_2303-9insGTTCCCCC (PEX1) NP_001269607.1:n.2303-10_2303-9insGTTCCCCC