Canonical Allele Identifier: CA2576747132
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521857dup , CM000681.2:g.33521857dup GRCh38
NC_000019.9:g.34012763dup , CM000681.1:g.34012763dup GRCh37
NC_000019.8:g.38704603dup NCBI36
NG_013358.1:g.5040dup
NG_013358.2:g.5040dup

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-94dup NP_000276.2:n.-94dup
NM_001166056.1:c.-94dup NP_001159528.1:n.-94dup
NM_001166057.1:c.-94dup NP_001159529.1:n.-94dup