Canonical Allele Identifier: CA2332698611

Gene: PEPD

Linked Data

• dbSNP Id: rs1968103310

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387510_33387512dup , CM000681.2:g.33387510_33387512dup	GRCh38
NC_000019.9:g.33878416_33878418dup , CM000681.1:g.33878416_33878418dup	GRCh37
NC_000019.8:g.38570256_38570258dup	NCBI36
NG_013358.1:g.139384_139386dup
NG_013358.2:g.139384_139386dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1411-29_1411-27dup	ENSP00000468516.4:n.1411-29_1411-27dup
ENST00000651901.2:c.1435-29_1435-27dup	ENSP00000498922.2:n.1435-29_1435-27dup
ENST00000698359.1:c.1300-29_1300-27dup	ENSP00000513682.1:n.1300-29_1300-27dup
ENST00000698360.1:c.1396-29_1396-27dup	ENSP00000513683.1:n.1396-29_1396-27dup
ENST00000698361.1:c.1461-29_1461-27dup	ENSP00000513684.1:n.1461-29_1461-27dup
ENST00000698362.1:c.*453_*455dup	ENSP00000513685.1:n.*453_*455dup
ENST00000698426.1:c.1024-29_1024-27dup	ENSP00000513713.1:n.1024-29_1024-27dup
ENST00000698427.1:c.1387-29_1387-27dup	ENSP00000513714.1:n.1387-29_1387-27dup
ENST00000698428.1:c.1024-29_1024-27dup	ENSP00000513715.1:n.1024-29_1024-27dup
ENST00000698429.1:n.1228-29_1228-27dup
ENST00000698430.1:c.1595-29_1595-27dup
ENST00000698431.1:c.1082-29_1082-27dup	ENSP00000513717.1:n.1082-29_1082-27dup
ENST00000698432.1:c.1154-29_1154-27dup
ENST00000698433.1:n.807-29_807-27dup
ENST00000244137.12:c.1345-29_1345-27dup MANE Select	ENSP00000244137.5:n.1345-29_1345-27dup
ENST00000588328.6:c.1400-29_1400-27dup
ENST00000651901.1:c.1431-29_1431-27dup
ENST00000244137.11:c.1345-29_1345-27dup	ENSP00000244137.5:n.1345-29_1345-27dup
ENST00000397032.8:c.1222-29_1222-27dup	ENSP00000380226.3:n.1222-29_1222-27dup
ENST00000436370.7:c.1153-29_1153-27dup	ENSP00000391890.2:n.1153-29_1153-27dup
ENST00000589598.5:n.70-29_70-27dup
ENST00000591968.1:n.417-29_417-27dup
ENST00000593085.1:n.1232-29_1232-27dup
NM_000285.3:c.1345-29_1345-27dup	NP_000276.2:n.1345-29_1345-27dup
NM_001166056.1:c.1222-29_1222-27dup	NP_001159528.1:n.1222-29_1222-27dup
NM_001166057.1:c.1153-29_1153-27dup	NP_001159529.1:n.1153-29_1153-27dup
NM_000285.4:c.1345-29_1345-27dup MANE Select	NP_000276.2:n.1345-29_1345-27dup
NM_001166056.2:c.1222-29_1222-27dup	NP_001159528.1:n.1222-29_1222-27dup
NM_001166057.2:c.1153-29_1153-27dup	NP_001159529.1:n.1153-29_1153-27dup