Canonical Allele Identifier: CA2332698508

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387338C= , CM000681.2:g.33387338C=	GRCh38
NC_000019.9:g.33878244C= , CM000681.1:g.33878244C=	GRCh37
NC_000019.8:g.38570084C=	NCBI36
NG_013358.1:g.139556G=
NG_013358.2:g.139556G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.*6G=	ENSP00000468516.4:n.*6G=
ENST00000651901.2:c.*6G=	ENSP00000498922.2:n.*6G=
ENST00000698359.1:c.*6G=	ENSP00000513682.1:n.*6G=
ENST00000698360.1:c.*6G=	ENSP00000513683.1:n.*6G=
ENST00000698361.1:c.*116G=	ENSP00000513684.1:n.*116G=
ENST00000698362.1:c.*625G=	ENSP00000513685.1:n.*625G=
ENST00000698426.1:c.*6G=	ENSP00000513713.1:n.*6G=
ENST00000698427.1:c.*6G=	ENSP00000513714.1:n.*6G=
ENST00000698428.1:c.*6G=	ENSP00000513715.1:n.*6G=
ENST00000698429.1:n.1371G=
ENST00000698430.1:c.1738G=
ENST00000698431.1:c.1225G=	ENSP00000513717.1:n.1225G=
ENST00000698432.1:c.1297G=
ENST00000244137.12:c.*6G= MANE Select	ENSP00000244137.5:n.*6G=
ENST00000588328.6:c.1543G=
ENST00000651901.1:c.1574G=
ENST00000244137.11:c.*6G=	ENSP00000244137.5:n.*6G=
ENST00000397032.8:c.*6G=	ENSP00000380226.3:n.*6G=
ENST00000436370.7:c.*6G=	ENSP00000391890.2:n.*6G=
ENST00000589598.5:n.213G=
ENST00000591968.1:n.560G=
ENST00000593085.1:n.1375G=
NM_000285.3:c.*6G=	NP_000276.2:n.*6G=
NM_001166056.1:c.*6G=	NP_001159528.1:n.*6G=
NM_001166057.1:c.*6G=	NP_001159529.1:n.*6G=
NM_000285.4:c.*6G= MANE Select	NP_000276.2:n.*6G=
NM_001166056.2:c.*6G=	NP_001159528.1:n.*6G=
NM_001166057.2:c.*6G=	NP_001159529.1:n.*6G=