Canonical Allele Identifier: CA405219776

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878384G>T (hg19) ; chr19:g.33387478G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387478G>T , CM000681.2:g.33387478G>T	GRCh38
NC_000019.9:g.33878384G>T , CM000681.1:g.33878384G>T	GRCh37
NC_000019.8:g.38570224G>T	NCBI36
NG_013358.1:g.139416C>A
NG_013358.2:g.139416C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.1414C>A	ENSP00000468516.4:p.Arg472Ser
ENST00000651901.2:c.1438C>A	ENSP00000498922.2:p.Arg480Ser
ENST00000698359.1:c.1303C>A	ENSP00000513682.1:p.Arg435Ser
ENST00000698360.1:c.1399C>A	ENSP00000513683.1:p.Arg467Ser
ENST00000698361.1:c.1464C>A	ENSP00000513684.1:p.Ser488=
ENST00000698362.1:c.*485C>A	ENSP00000513685.1:n.*485C>A
ENST00000698426.1:c.1027C>A	ENSP00000513713.1:p.Arg343Ser
ENST00000698427.1:c.1390C>A	ENSP00000513714.1:p.Arg464Ser
ENST00000698428.1:c.1027C>A	ENSP00000513715.1:p.Arg343Ser
ENST00000698429.1:n.1231C>A
ENST00000698430.1:c.1598C>A
ENST00000698431.1:c.1085C>A	ENSP00000513717.1:n.1085C>A
ENST00000698432.1:c.1157C>A
ENST00000698433.1:n.810C>A
ENST00000244137.12:c.1348C>A MANE Select	ENSP00000244137.5:p.Arg450Ser
ENST00000588328.6:c.1403C>A
ENST00000651901.1:c.1434C>A
ENST00000244137.11:c.1348C>A	ENSP00000244137.5:p.Arg450Ser
ENST00000397032.8:c.1225C>A	ENSP00000380226.3:p.Arg409Ser
ENST00000436370.7:c.1156C>A	ENSP00000391890.2:p.Arg386Ser
ENST00000589598.5:n.73C>A
ENST00000591968.1:n.420C>A
ENST00000593085.1:n.1235C>A
NM_000285.3:c.1348C>A	NP_000276.2:p.Arg450Ser
NM_001166056.1:c.1225C>A	NP_001159528.1:p.Arg409Ser
NM_001166057.1:c.1156C>A	NP_001159529.1:p.Arg386Ser
NM_000285.4:c.1348C>A MANE Select	NP_000276.2:p.Arg450Ser
NM_001166056.2:c.1225C>A	NP_001159528.1:p.Arg409Ser
NM_001166057.2:c.1156C>A	NP_001159529.1:p.Arg386Ser