Canonical Allele Identifier: CA2584321375

Gene: PEPD

Linked Data

• gnomAD v4: 19-33387249-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387249_33387250insC , CM000681.2:g.33387249_33387250insC	GRCh38
NC_000019.9:g.33878155_33878156insC , CM000681.1:g.33878155_33878156insC	GRCh37
NC_000019.8:g.38569995_38569996insC	NCBI36
NG_013358.1:g.139644_139645insG
NG_013358.2:g.139644_139645insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.*94_*95insG	ENSP00000468516.4:n.*94_*95insG
ENST00000651901.2:c.*94_*95insG	ENSP00000498922.2:n.*94_*95insG
ENST00000698359.1:c.*94_*95insG	ENSP00000513682.1:n.*94_*95insG
ENST00000698360.1:c.*94_*95insG	ENSP00000513683.1:n.*94_*95insG
ENST00000698361.1:c.*204_*205insG	ENSP00000513684.1:n.*204_*205insG
ENST00000698362.1:c.*713_*714insG	ENSP00000513685.1:n.*713_*714insG
ENST00000698426.1:c.*94_*95insG	ENSP00000513713.1:n.*94_*95insG
ENST00000698427.1:c.*94_*95insG	ENSP00000513714.1:n.*94_*95insG
ENST00000698428.1:c.*94_*95insG	ENSP00000513715.1:n.*94_*95insG
ENST00000698429.1:n.1459_1460insG
ENST00000698430.1:c.1826_1827insG
ENST00000698431.1:c.1313_1314insG	ENSP00000513717.1:n.1313_1314insG
ENST00000698432.1:c.1385_1386insG
ENST00000244137.12:c.*94_*95insG MANE Select	ENSP00000244137.5:n.*94_*95insG
ENST00000588328.6:c.1631_1632insG
ENST00000651901.1:c.1662_1663insG
ENST00000244137.11:c.*94_*95insG	ENSP00000244137.5:n.*94_*95insG
ENST00000397032.8:c.*94_*95insG	ENSP00000380226.3:n.*94_*95insG
ENST00000436370.7:c.*94_*95insG	ENSP00000391890.2:n.*94_*95insG
ENST00000589598.5:n.301_302insG
ENST00000591968.1:n.648_649insG
ENST00000593085.1:n.1463_1464insG
NM_000285.3:c.*94_*95insG	NP_000276.2:n.*94_*95insG
NM_001166056.1:c.*94_*95insG	NP_001159528.1:n.*94_*95insG
NM_001166057.1:c.*94_*95insG	NP_001159529.1:n.*94_*95insG
NM_000285.4:c.*94_*95insG MANE Select	NP_000276.2:n.*94_*95insG
NM_001166056.2:c.*94_*95insG	NP_001159528.1:n.*94_*95insG
NM_001166057.2:c.*94_*95insG	NP_001159529.1:n.*94_*95insG