Canonical Allele Identifier: CA2584327926
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521834dup , CM000681.2:g.33521834dup GRCh38
NC_000019.9:g.34012740dup , CM000681.1:g.34012740dup GRCh37
NC_000019.8:g.38704580dup NCBI36
NG_013358.1:g.5063dup
NG_013358.2:g.5063dup

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-71dup NP_000276.2:n.-71dup
NM_001166056.1:c.-71dup NP_001159528.1:n.-71dup
NM_001166057.1:c.-71dup NP_001159529.1:n.-71dup