Canonical Allele Identifier: CA2332763194
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521847_33521848delinsAG , CM000681.2:g.33521847_33521848delinsAG GRCh38
NC_000019.9:g.34012753_34012754delinsAG , CM000681.1:g.34012753_34012754delinsAG GRCh37
NC_000019.8:g.38704593_38704594delinsAG NCBI36
NG_013358.1:g.5046_5047delinsCT
NG_013358.2:g.5046_5047delinsCT

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-88_-87delinsCT NP_000276.2:n.-88_-87delinsCT
NM_001166056.1:c.-88_-87delinsCT NP_001159528.1:n.-88_-87delinsCT
NM_001166057.1:c.-88_-87delinsCT NP_001159529.1:n.-88_-87delinsCT