Canonical Allele Identifier: CA881598388

Gene: PEPD

Linked Data

• dbSNP Id: rs1166526638
• gnomAD v3: 19-33387581-C-T
• gnomAD v4: 19-33387581-C-T
• MyVariant Identifiers: chr19:g.33878487C>T (hg19) ; chr19:g.33387581C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387581C>T , CM000681.2:g.33387581C>T	GRCh38
NC_000019.9:g.33878487C>T , CM000681.1:g.33878487C>T	GRCh37
NC_000019.8:g.38570327C>T	NCBI36
NG_013358.1:g.139313G>A
NG_013358.2:g.139313G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1411-100G>A	ENSP00000468516.4:n.1411-100G>A
ENST00000651901.2:c.1434+74G>A	ENSP00000498922.2:n.1434+74G>A
ENST00000698359.1:c.1300-100G>A	ENSP00000513682.1:n.1300-100G>A
ENST00000698360.1:c.1396-100G>A	ENSP00000513683.1:n.1396-100G>A
ENST00000698361.1:c.1461-100G>A	ENSP00000513684.1:n.1461-100G>A
ENST00000698362.1:c.*382G>A	ENSP00000513685.1:n.*382G>A
ENST00000698426.1:c.1024-100G>A	ENSP00000513713.1:n.1024-100G>A
ENST00000698427.1:c.1387-100G>A	ENSP00000513714.1:n.1387-100G>A
ENST00000698428.1:c.1024-100G>A	ENSP00000513715.1:n.1024-100G>A
ENST00000698429.1:n.1228-100G>A
ENST00000698430.1:c.1595-100G>A
ENST00000698431.1:c.1082-100G>A	ENSP00000513717.1:n.1082-100G>A
ENST00000698432.1:c.1154-100G>A
ENST00000698433.1:n.807-100G>A
ENST00000244137.12:c.1345-100G>A MANE Select	ENSP00000244137.5:n.1345-100G>A
ENST00000588328.6:c.1400-100G>A
ENST00000651901.1:c.1430+74G>A
ENST00000244137.11:c.1345-100G>A	ENSP00000244137.5:n.1345-100G>A
ENST00000397032.8:c.1222-100G>A	ENSP00000380226.3:n.1222-100G>A
ENST00000436370.7:c.1153-100G>A	ENSP00000391890.2:n.1153-100G>A
ENST00000589598.5:n.69+74G>A
ENST00000591968.1:n.417-100G>A
ENST00000593085.1:n.1232-100G>A
NM_000285.3:c.1345-100G>A	NP_000276.2:n.1345-100G>A
NM_001166056.1:c.1222-100G>A	NP_001159528.1:n.1222-100G>A
NM_001166057.1:c.1153-100G>A	NP_001159529.1:n.1153-100G>A
NM_000285.4:c.1345-100G>A MANE Select	NP_000276.2:n.1345-100G>A
NM_001166056.2:c.1222-100G>A	NP_001159528.1:n.1222-100G>A
NM_001166057.2:c.1153-100G>A	NP_001159529.1:n.1153-100G>A