Canonical Allele Identifier: CA2584327949
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521843_33521844insC , CM000681.2:g.33521843_33521844insC GRCh38
NC_000019.9:g.34012749_34012750insC , CM000681.1:g.34012749_34012750insC GRCh37
NC_000019.8:g.38704589_38704590insC NCBI36
NG_013358.1:g.5050_5051insG
NG_013358.2:g.5050_5051insG

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-84_-83insG NP_000276.2:n.-84_-83insG
NM_001166056.1:c.-84_-83insG NP_001159528.1:n.-84_-83insG
NM_001166057.1:c.-84_-83insG NP_001159529.1:n.-84_-83insG