Canonical Allele Identifier: CA2735810306
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs2145369737

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521844_33521846dup , CM000681.2:g.33521844_33521846dup GRCh38
NC_000019.9:g.34012750_34012752dup , CM000681.1:g.34012750_34012752dup GRCh37
NC_000019.8:g.38704590_38704592dup NCBI36
NG_013358.1:g.5048_5050dup
NG_013358.2:g.5048_5050dup

Transcript Alleles

HGVS Amino-acid Change
NM_000285.3:c.-86_-84dup NP_000276.2:n.-86_-84dup
NM_001166056.1:c.-86_-84dup NP_001159528.1:n.-86_-84dup
NM_001166057.1:c.-86_-84dup NP_001159529.1:n.-86_-84dup