Canonical Allele Identifier: CA2332763209
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521871_33521872delinsAC , CM000681.2:g.33521871_33521872delinsAC GRCh38
NC_000019.9:g.34012777_34012778delinsAC , CM000681.1:g.34012777_34012778delinsAC GRCh37
NC_000019.8:g.38704617_38704618delinsAC NCBI36
NG_013358.1:g.5022_5023delinsGT
NG_013358.2:g.5022_5023delinsGT

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-112_-111delinsGT NP_000276.2:n.-112_-111delinsGT
NM_001166056.1:c.-112_-111delinsGT NP_001159528.1:n.-112_-111delinsGT
NM_001166057.1:c.-112_-111delinsGT NP_001159529.1:n.-112_-111delinsGT