Canonical Allele Identifier: CA2332763195

Gene: PEPD

Linked Data

• dbSNP Id: rs1971150579
• gnomAD v4: 19-33521847-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521852del , CM000681.2:g.33521852del	GRCh38
NC_000019.9:g.34012758del , CM000681.1:g.34012758del	GRCh37
NC_000019.8:g.38704598del	NCBI36
NG_013358.1:g.5046del
NG_013358.2:g.5046del

Transcript Alleles

HGVS	Amino-acid Change
NM_000285.3:c.-88del	NP_000276.2:n.-88del
NM_001166056.1:c.-88del	NP_001159528.1:n.-88del
NM_001166057.1:c.-88del	NP_001159529.1:n.-88del