Canonical Allele Identifier: CA2332763169

Gene: PEPD

Linked Data

• dbSNP Id: rs1971148556
• gnomAD v4: 19-33521806-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521806C>A , CM000681.2:g.33521806C>A	GRCh38
NC_000019.9:g.34012712C>A , CM000681.1:g.34012712C>A	GRCh37
NC_000019.8:g.38704552C>A	NCBI36
NG_013358.1:g.5088G>T
NG_013358.2:g.5088G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698361.1:c.-46G>T	ENSP00000513684.1:n.-46G>T
ENST00000698362.1:c.-46G>T	ENSP00000513685.1:n.-46G>T
ENST00000698363.1:n.18G>T
ENST00000698364.1:n.18G>T
ENST00000698365.1:n.18G>T
ENST00000698436.1:c.-46G>T	ENSP00000513720.1:n.-46G>T
NM_000285.3:c.-46G>T	NP_000276.2:n.-46G>T
NM_001166056.1:c.-46G>T	NP_001159528.1:n.-46G>T
NM_001166057.1:c.-46G>T	NP_001159529.1:n.-46G>T