Canonical Allele Identifier: CA2584327910
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521823C>A , CM000681.2:g.33521823C>A GRCh38
NC_000019.9:g.34012729C>A , CM000681.1:g.34012729C>A GRCh37
NC_000019.8:g.38704569C>A NCBI36
NG_013358.1:g.5071G>T
NG_013358.2:g.5071G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698361.1:c.-63G>T ENSP00000513684.1:n.-63G>T
ENST00000698362.1:c.-63G>T ENSP00000513685.1:n.-63G>T
ENST00000698363.1:n.1G>T
ENST00000698364.1:n.1G>T
ENST00000698365.1:n.1G>T
NM_000285.3:c.-63G>T NP_000276.2:n.-63G>T
NM_001166056.1:c.-63G>T NP_001159528.1:n.-63G>T
NM_001166057.1:c.-63G>T NP_001159529.1:n.-63G>T