Canonical Allele Identifier: CA2332698569

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387456A= , CM000681.2:g.33387456A=	GRCh38
NC_000019.9:g.33878362A= , CM000681.1:g.33878362A=	GRCh37
NC_000019.8:g.38570202A=	NCBI36
NG_013358.1:g.139438T=
NG_013358.2:g.139438T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1436T=	ENSP00000468516.4:p.Val479=
ENST00000651901.2:c.1460T=	ENSP00000498922.2:p.Val487=
ENST00000698359.1:c.1325T=	ENSP00000513682.1:p.Val442=
ENST00000698360.1:c.1421T=	ENSP00000513683.1:p.Val474=
ENST00000698361.1:c.1486T=	ENSP00000513684.1:p.Ter496=
ENST00000698362.1:c.*507T=	ENSP00000513685.1:n.*507T=
ENST00000698426.1:c.1049T=	ENSP00000513713.1:p.Val350=
ENST00000698427.1:c.1412T=	ENSP00000513714.1:p.Val471=
ENST00000698428.1:c.1049T=	ENSP00000513715.1:p.Val350=
ENST00000698429.1:n.1253T=
ENST00000698430.1:c.1620T=
ENST00000698431.1:c.1107T=	ENSP00000513717.1:n.1107T=
ENST00000698432.1:c.1179T=
ENST00000698433.1:n.832T=
ENST00000244137.12:c.1370T= MANE Select	ENSP00000244137.5:p.Val457=
ENST00000588328.6:c.1425T=
ENST00000651901.1:c.1456T=
ENST00000244137.11:c.1370T=	ENSP00000244137.5:p.Val457=
ENST00000397032.8:c.1247T=	ENSP00000380226.3:p.Val416=
ENST00000436370.7:c.1178T=	ENSP00000391890.2:p.Val393=
ENST00000589598.5:n.95T=
ENST00000591968.1:n.442T=
ENST00000593085.1:n.1257T=
NM_000285.3:c.1370T=	NP_000276.2:p.Val457=
NM_001166056.1:c.1247T=	NP_001159528.1:p.Val416=
NM_001166057.1:c.1178T=	NP_001159529.1:p.Val393=
NM_000285.4:c.1370T= MANE Select	NP_000276.2:p.Val457=
NM_001166056.2:c.1247T=	NP_001159528.1:p.Val416=
NM_001166057.2:c.1178T=	NP_001159529.1:p.Val393=