Canonical Allele Identifier: CA2332763214
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521880C= , CM000681.2:g.33521880C= GRCh38
NC_000019.9:g.34012786C= , CM000681.1:g.34012786C= GRCh37
NC_000019.8:g.38704626C= NCBI36
NG_013358.1:g.5014G=
NG_013358.2:g.5014G=

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-120G= NP_000276.2:n.-120G=
NM_001166056.1:c.-120G= NP_001159528.1:n.-120G=
NM_001166057.1:c.-120G= NP_001159529.1:n.-120G=