Canonical Allele Identifier: CA2332763185
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521831G= , CM000681.2:g.33521831G= GRCh38
NC_000019.9:g.34012737G= , CM000681.1:g.34012737G= GRCh37
NC_000019.8:g.38704577G= NCBI36
NG_013358.1:g.5063C=
NG_013358.2:g.5063C=

Transcript Alleles

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