Canonical Allele Identifier: CA2332763153
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521792_33521798delinsGGCGTCA , CM000681.2:g.33521792_33521798delinsGGCGTCA GRCh38
NC_000019.9:g.34012698_34012704delinsGGCGTCA , CM000681.1:g.34012698_34012704delinsGGCGTCA GRCh37
NC_000019.8:g.38704538_38704544delinsGGCGTCA NCBI36
NG_013358.1:g.5096_5102delinsTGACGCC
NG_013358.2:g.5096_5102delinsTGACGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000698361.1:c.-38_-32delinsTGACGCC ENSP00000513684.1:n.-38_-32delinsTGACGCC
ENST00000698362.1:c.-38_-32delinsTGACGCC ENSP00000513685.1:n.-38_-32delinsTGACGCC
ENST00000698363.1:n.26_32delinsTGACGCC
ENST00000698364.1:n.26_32delinsTGACGCC
ENST00000698365.1:n.26_32delinsTGACGCC
ENST00000698436.1:c.-38_-32delinsTGACGCC ENSP00000513720.1:n.-38_-32delinsTGACGCC
NM_000285.3:c.-38_-32delinsTGACGCC NP_000276.2:n.-38_-32delinsTGACGCC
NM_001166056.1:c.-38_-32delinsTGACGCC NP_001159528.1:n.-38_-32delinsTGACGCC
NM_001166057.1:c.-38_-32delinsTGACGCC NP_001159529.1:n.-38_-32delinsTGACGCC