Canonical Allele Identifier: CA2332698450

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387239T= , CM000681.2:g.33387239T=	GRCh38
NC_000019.9:g.33878145T= , CM000681.1:g.33878145T=	GRCh37
NC_000019.8:g.38569985T=	NCBI36
NG_013358.1:g.139655A=
NG_013358.2:g.139655A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.*105A=	ENSP00000468516.4:n.*105A=
ENST00000651901.2:c.*105A=	ENSP00000498922.2:n.*105A=
ENST00000698359.1:c.*105A=	ENSP00000513682.1:n.*105A=
ENST00000698360.1:c.*105A=	ENSP00000513683.1:n.*105A=
ENST00000698361.1:c.*215A=	ENSP00000513684.1:n.*215A=
ENST00000698362.1:c.*724A=	ENSP00000513685.1:n.*724A=
ENST00000698426.1:c.*105A=	ENSP00000513713.1:n.*105A=
ENST00000698427.1:c.*105A=	ENSP00000513714.1:n.*105A=
ENST00000698428.1:c.*105A=	ENSP00000513715.1:n.*105A=
ENST00000698429.1:n.1470A=
ENST00000698430.1:c.1837A=
ENST00000698431.1:c.1324A=	ENSP00000513717.1:n.1324A=
ENST00000698432.1:c.1396A=
ENST00000244137.12:c.*105A= MANE Select	ENSP00000244137.5:n.*105A=
ENST00000588328.6:c.1642A=
ENST00000651901.1:c.1673A=
ENST00000244137.11:c.*105A=	ENSP00000244137.5:n.*105A=
ENST00000397032.8:c.*105A=	ENSP00000380226.3:n.*105A=
ENST00000436370.7:c.*105A=	ENSP00000391890.2:n.*105A=
ENST00000589598.5:n.312A=
ENST00000591968.1:n.659A=
ENST00000593085.1:n.1474A=
NM_000285.3:c.*105A=	NP_000276.2:n.*105A=
NM_001166056.1:c.*105A=	NP_001159528.1:n.*105A=
NM_001166057.1:c.*105A=	NP_001159529.1:n.*105A=
NM_000285.4:c.*105A= MANE Select	NP_000276.2:n.*105A=
NM_001166056.2:c.*105A=	NP_001159528.1:n.*105A=
NM_001166057.2:c.*105A=	NP_001159529.1:n.*105A=