Canonical Allele Identifier: CA2332763157
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521795G= , CM000681.2:g.33521795G= GRCh38
NC_000019.9:g.34012701G= , CM000681.1:g.34012701G= GRCh37
NC_000019.8:g.38704541G= NCBI36
NG_013358.1:g.5099C=
NG_013358.2:g.5099C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698360.1:c.-35C= ENSP00000513683.1:n.-35C=
ENST00000698361.1:c.-35C= ENSP00000513684.1:n.-35C=
ENST00000698362.1:c.-35C= ENSP00000513685.1:n.-35C=
ENST00000698363.1:n.29C=
ENST00000698364.1:n.29C=
ENST00000698365.1:n.29C=
ENST00000698436.1:c.-35C= ENSP00000513720.1:n.-35C=
NM_000285.3:c.-35C= NP_000276.2:n.-35C=
NM_001166056.1:c.-35C= NP_001159528.1:n.-35C=
NM_001166057.1:c.-35C= NP_001159529.1:n.-35C=