Canonical Allele Identifier: CA2332698490

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387301T= , CM000681.2:g.33387301T=	GRCh38
NC_000019.9:g.33878207T= , CM000681.1:g.33878207T=	GRCh37
NC_000019.8:g.38570047T=	NCBI36
NG_013358.1:g.139593A=
NG_013358.2:g.139593A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.*43A=	ENSP00000468516.4:n.*43A=
ENST00000651901.2:c.*43A=	ENSP00000498922.2:n.*43A=
ENST00000698359.1:c.*43A=	ENSP00000513682.1:n.*43A=
ENST00000698360.1:c.*43A=	ENSP00000513683.1:n.*43A=
ENST00000698361.1:c.*153A=	ENSP00000513684.1:n.*153A=
ENST00000698362.1:c.*662A=	ENSP00000513685.1:n.*662A=
ENST00000698426.1:c.*43A=	ENSP00000513713.1:n.*43A=
ENST00000698427.1:c.*43A=	ENSP00000513714.1:n.*43A=
ENST00000698428.1:c.*43A=	ENSP00000513715.1:n.*43A=
ENST00000698429.1:n.1408A=
ENST00000698430.1:c.1775A=
ENST00000698431.1:c.1262A=	ENSP00000513717.1:n.1262A=
ENST00000698432.1:c.1334A=
ENST00000244137.12:c.*43A= MANE Select	ENSP00000244137.5:n.*43A=
ENST00000588328.6:c.1580A=
ENST00000651901.1:c.1611A=
ENST00000244137.11:c.*43A=	ENSP00000244137.5:n.*43A=
ENST00000397032.8:c.*43A=	ENSP00000380226.3:n.*43A=
ENST00000436370.7:c.*43A=	ENSP00000391890.2:n.*43A=
ENST00000589598.5:n.250A=
ENST00000591968.1:n.597A=
ENST00000593085.1:n.1412A=
NM_000285.3:c.*43A=	NP_000276.2:n.*43A=
NM_001166056.1:c.*43A=	NP_001159528.1:n.*43A=
NM_001166057.1:c.*43A=	NP_001159529.1:n.*43A=
NM_000285.4:c.*43A= MANE Select	NP_000276.2:n.*43A=
NM_001166056.2:c.*43A=	NP_001159528.1:n.*43A=
NM_001166057.2:c.*43A=	NP_001159529.1:n.*43A=