Canonical Allele Identifier: CA2332763198
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521851G= , CM000681.2:g.33521851G= GRCh38
NC_000019.9:g.34012757G= , CM000681.1:g.34012757G= GRCh37
NC_000019.8:g.38704597G= NCBI36
NG_013358.1:g.5043C=
NG_013358.2:g.5043C=

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-91C= NP_000276.2:n.-91C=
NM_001166056.1:c.-91C= NP_001159528.1:n.-91C=
NM_001166057.1:c.-91C= NP_001159529.1:n.-91C=