Canonical Allele Identifier: CA2332763193
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521846C= , CM000681.2:g.33521846C= GRCh38
NC_000019.9:g.34012752C= , CM000681.1:g.34012752C= GRCh37
NC_000019.8:g.38704592C= NCBI36
NG_013358.1:g.5048G=
NG_013358.2:g.5048G=

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-86G= NP_000276.2:n.-86G=
NM_001166056.1:c.-86G= NP_001159528.1:n.-86G=
NM_001166057.1:c.-86G= NP_001159529.1:n.-86G=