Canonical Allele Identifier: CA506686771

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878322G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387416G>C , CM000681.2:g.33387416G>C	GRCh38
NC_000019.9:g.33878322G>C , CM000681.1:g.33878322G>C	GRCh37
NC_000019.8:g.38570162G>C	NCBI36
NG_013358.1:g.139478C>G
NG_013358.2:g.139478C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1476C>G	ENSP00000468516.4:p.Arg492=
ENST00000651901.2:c.1500C>G	ENSP00000498922.2:p.Arg500=
ENST00000698359.1:c.1365C>G	ENSP00000513682.1:p.Arg455=
ENST00000698360.1:c.1461C>G	ENSP00000513683.1:p.Arg487=
ENST00000698361.1:c.*38C>G	ENSP00000513684.1:n.*38C>G
ENST00000698362.1:c.*547C>G	ENSP00000513685.1:n.*547C>G
ENST00000698426.1:c.1089C>G	ENSP00000513713.1:p.Arg363=
ENST00000698427.1:c.1452C>G	ENSP00000513714.1:p.Arg484=
ENST00000698428.1:c.1089C>G	ENSP00000513715.1:p.Arg363=
ENST00000698429.1:n.1293C>G
ENST00000698430.1:c.1660C>G
ENST00000698431.1:c.1147C>G	ENSP00000513717.1:n.1147C>G
ENST00000698432.1:c.1219C>G
ENST00000698433.1:n.872C>G
ENST00000244137.12:c.1410C>G MANE Select	ENSP00000244137.5:p.Arg470=
ENST00000588328.6:c.1465C>G
ENST00000651901.1:c.1496C>G
ENST00000244137.11:c.1410C>G	ENSP00000244137.5:p.Arg470=
ENST00000397032.8:c.1287C>G	ENSP00000380226.3:p.Arg429=
ENST00000436370.7:c.1218C>G	ENSP00000391890.2:p.Arg406=
ENST00000589598.5:n.135C>G
ENST00000591968.1:n.482C>G
ENST00000593085.1:n.1297C>G
NM_000285.3:c.1410C>G	NP_000276.2:p.Arg470=
NM_001166056.1:c.1287C>G	NP_001159528.1:p.Arg429=
NM_001166057.1:c.1218C>G	NP_001159529.1:p.Arg406=
NM_000285.4:c.1410C>G MANE Select	NP_000276.2:p.Arg470=
NM_001166056.2:c.1287C>G	NP_001159528.1:p.Arg429=
NM_001166057.2:c.1218C>G	NP_001159529.1:p.Arg406=