Canonical Allele Identifier: CA2576747100
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521824_33521825insC , CM000681.2:g.33521824_33521825insC GRCh38
NC_000019.9:g.34012730_34012731insC , CM000681.1:g.34012730_34012731insC GRCh37
NC_000019.8:g.38704570_38704571insC NCBI36
NG_013358.1:g.5069_5070insG
NG_013358.2:g.5069_5070insG

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-65_-64insG NP_000276.2:n.-65_-64insG
NM_001166056.1:c.-65_-64insG NP_001159528.1:n.-65_-64insG
NM_001166057.1:c.-65_-64insG NP_001159529.1:n.-65_-64insG