Canonical Allele Identifier: CA2332735660
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33464009_33464010delinsAT , CM000681.2:g.33464009_33464010delinsAT GRCh38
NC_000019.9:g.33954915_33954916delinsAT , CM000681.1:g.33954915_33954916delinsAT GRCh37
NC_000019.8:g.38646755_38646756delinsAT NCBI36
NG_013358.1:g.62884_62885delinsAT
NG_013358.2:g.62884_62885delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000588328.7:c.601_602delinsAT ENSP00000468516.4:p.Ile201=
ENST00000651646.2:c.601_602delinsAT ENSP00000498950.2:p.Ile201=
ENST00000651901.2:c.601_602delinsAT ENSP00000498922.2:p.Ile201=
ENST00000698359.1:c.556_557delinsAT ENSP00000513682.1:p.Ile186=
ENST00000698360.1:c.601_602delinsAT ENSP00000513683.1:p.Ile201=
ENST00000698361.1:c.601_602delinsAT ENSP00000513684.1:p.Ile201=
ENST00000698362.1:c.601_602delinsAT ENSP00000513685.1:p.Ile201=
ENST00000698363.1:n.664_665delinsAT
ENST00000698364.1:n.664_665delinsAT
ENST00000698365.1:n.664_665delinsAT
ENST00000698426.1:c.280_281delinsAT ENSP00000513713.1:p.Ile94=
ENST00000698427.1:c.643_644delinsAT ENSP00000513714.1:p.Ile215=
ENST00000698428.1:c.280_281delinsAT ENSP00000513715.1:p.Ile94=
ENST00000698430.1:c.851_852delinsAT
ENST00000698431.1:c.338_339delinsAT ENSP00000513717.1:n.338_339delinsAT
ENST00000698432.1:c.410_411delinsAT
ENST00000698435.1:c.289_290delinsAT ENSP00000513719.1:p.Ile97=
ENST00000698436.1:c.*213_*214delinsAT ENSP00000513720.1:n.*213_*214delinsAT
ENST00000698437.1:n.584_585delinsAT
ENST00000698438.1:n.583_584delinsAT
ENST00000698439.1:c.458_459delinsAT ENSP00000513721.1:n.458_459delinsAT
ENST00000244137.12:c.601_602delinsAT MANE Select ENSP00000244137.5:p.Ile201=
ENST00000588328.6:c.590_591delinsAT
ENST00000590731.6:n.276_277delinsAT
ENST00000651646.1:c.599_600delinsAT
ENST00000651901.1:c.597_598delinsAT
ENST00000244137.11:c.601_602delinsAT ENSP00000244137.5:p.Ile201=
ENST00000397032.8:c.548+14036_548+14037delinsAT ENSP00000380226.3:n.548+14036_548+14037de...
ENST00000436370.7:c.409_410delinsAT ENSP00000391890.2:p.Ile137=
ENST00000588328.5:c.92_93delinsAT
ENST00000588719.5:n.236_237delinsAT
ENST00000590408.1:c.319_320delinsAT
ENST00000590731.5:n.276_277delinsAT
ENST00000590755.6:c.428_429delinsAT ENSP00000476667.1:n.428_429delinsAT
ENST00000593163.5:n.766_767delinsAT
ENST00000609145.5:c.34_35delinsAT ENSP00000476514.1:p.Ile12=
NM_000285.3:c.601_602delinsAT NP_000276.2:p.Ile201=
NM_001166056.1:c.548+14036_548+14037delinsAT NP_001159528.1:n.548+14036_548+14037delin...
NM_001166057.1:c.409_410delinsAT NP_001159529.1:p.Ile137=
NM_000285.4:c.601_602delinsAT MANE Select NP_000276.2:p.Ile201=
NM_001166056.2:c.548+14036_548+14037delinsAT NP_001159528.1:n.548+14036_548+14037delin...
NM_001166057.2:c.409_410delinsAT NP_001159529.1:p.Ile137=