Canonical Allele Identifier: CA995316479
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs1971147843
gnomAD v3: 19-33521794-C-T
gnomAD v4: 19-33521794-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521794C>T , CM000681.2:g.33521794C>T GRCh38
NC_000019.9:g.34012700C>T , CM000681.1:g.34012700C>T GRCh37
NC_000019.8:g.38704540C>T NCBI36
NG_013358.1:g.5100G>A
NG_013358.2:g.5100G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698360.1:c.-34G>A ENSP00000513683.1:n.-34G>A
ENST00000698361.1:c.-34G>A ENSP00000513684.1:n.-34G>A
ENST00000698362.1:c.-34G>A ENSP00000513685.1:n.-34G>A
ENST00000698363.1:n.30G>A
ENST00000698364.1:n.30G>A
ENST00000698365.1:n.30G>A
ENST00000698436.1:c.-34G>A ENSP00000513720.1:n.-34G>A
ENST00000244137.11:c.-34G>A ENSP00000244137.5:n.-34G>A
NM_000285.3:c.-34G>A NP_000276.2:n.-34G>A
NM_001166056.1:c.-34G>A NP_001159528.1:n.-34G>A
NM_001166057.1:c.-34G>A NP_001159529.1:n.-34G>A
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