Canonical Allele Identifier: CA2584327907
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521820A>G , CM000681.2:g.33521820A>G GRCh38
NC_000019.9:g.34012726A>G , CM000681.1:g.34012726A>G GRCh37
NC_000019.8:g.38704566A>G NCBI36
NG_013358.1:g.5074T>C
NG_013358.2:g.5074T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698361.1:c.-60T>C ENSP00000513684.1:n.-60T>C
ENST00000698362.1:c.-60T>C ENSP00000513685.1:n.-60T>C
ENST00000698363.1:n.4T>C
ENST00000698364.1:n.4T>C
ENST00000698365.1:n.4T>C
NM_000285.3:c.-60T>C NP_000276.2:n.-60T>C
NM_001166056.1:c.-60T>C NP_001159528.1:n.-60T>C
NM_001166057.1:c.-60T>C NP_001159529.1:n.-60T>C