Canonical Allele Identifier: CA2584327905

Gene: PEPD

Linked Data

• gnomAD v4: 19-33521819-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521819A>C , CM000681.2:g.33521819A>C	GRCh38
NC_000019.9:g.34012725A>C , CM000681.1:g.34012725A>C	GRCh37
NC_000019.8:g.38704565A>C	NCBI36
NG_013358.1:g.5075T>G
NG_013358.2:g.5075T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698361.1:c.-59T>G	ENSP00000513684.1:n.-59T>G
ENST00000698362.1:c.-59T>G	ENSP00000513685.1:n.-59T>G
ENST00000698363.1:n.5T>G
ENST00000698364.1:n.5T>G
ENST00000698365.1:n.5T>G
NM_000285.3:c.-59T>G	NP_000276.2:n.-59T>G
NM_001166056.1:c.-59T>G	NP_001159528.1:n.-59T>G
NM_001166057.1:c.-59T>G	NP_001159529.1:n.-59T>G