Canonical Allele Identifier: CA2576747108
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521836_33521837insCGGGGGGGGTA , CM000681.2:g.33521836_33521837insCGGGGGGGGTA GRCh38
NC_000019.9:g.34012742_34012743insCGGGGGGGGTA , CM000681.1:g.34012742_34012743insCGGGGGGGGTA GRCh37
NC_000019.8:g.38704582_38704583insCGGGGGGGGTA NCBI36
NG_013358.1:g.5063_5064insCCCCGTACCCC
NG_013358.2:g.5063_5064insCCCCGTACCCC

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-71_-70insCCCCGTACCCC NP_000276.2:n.-71_-70insCCCCGTACCCC
NM_001166056.1:c.-71_-70insCCCCGTACCCC NP_001159528.1:n.-71_-70insCCCCGTACCCC
NM_001166057.1:c.-71_-70insCCCCGTACCCC NP_001159529.1:n.-71_-70insCCCCGTACCCC