Canonical Allele Identifier: CA506687139

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33954917T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33464011T>C , CM000681.2:g.33464011T>C	GRCh38
NC_000019.9:g.33954917T>C , CM000681.1:g.33954917T>C	GRCh37
NC_000019.8:g.38646757T>C	NCBI36
NG_013358.1:g.62883A>G
NG_013358.2:g.62883A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.600A>G	ENSP00000468516.4:p.Lys200=
ENST00000651646.2:c.600A>G	ENSP00000498950.2:p.Lys200=
ENST00000651901.2:c.600A>G	ENSP00000498922.2:p.Lys200=
ENST00000698359.1:c.555A>G	ENSP00000513682.1:p.Lys185=
ENST00000698360.1:c.600A>G	ENSP00000513683.1:p.Lys200=
ENST00000698361.1:c.600A>G	ENSP00000513684.1:p.Lys200=
ENST00000698362.1:c.600A>G	ENSP00000513685.1:p.Lys200=
ENST00000698363.1:n.663A>G
ENST00000698364.1:n.663A>G
ENST00000698365.1:n.663A>G
ENST00000698426.1:c.279A>G	ENSP00000513713.1:p.Lys93=
ENST00000698427.1:c.642A>G	ENSP00000513714.1:p.Lys214=
ENST00000698428.1:c.279A>G	ENSP00000513715.1:p.Lys93=
ENST00000698430.1:c.850A>G
ENST00000698431.1:c.337A>G	ENSP00000513717.1:n.337A>G
ENST00000698432.1:c.409A>G
ENST00000698435.1:c.288A>G	ENSP00000513719.1:p.Lys96=
ENST00000698436.1:c.*212A>G	ENSP00000513720.1:n.*212A>G
ENST00000698437.1:n.583A>G
ENST00000698438.1:n.582A>G
ENST00000698439.1:c.457A>G	ENSP00000513721.1:n.457A>G
ENST00000244137.12:c.600A>G MANE Select	ENSP00000244137.5:p.Lys200=
ENST00000588328.6:c.589A>G
ENST00000590731.6:n.275A>G
ENST00000651646.1:c.598A>G
ENST00000651901.1:c.596A>G
ENST00000244137.11:c.600A>G	ENSP00000244137.5:p.Lys200=
ENST00000397032.8:c.548+14035A>G	ENSP00000380226.3:n.548+14035A>G
ENST00000436370.7:c.408A>G	ENSP00000391890.2:p.Lys136=
ENST00000588328.5:c.91A>G
ENST00000588719.5:n.235A>G
ENST00000590408.1:c.318A>G
ENST00000590731.5:n.275A>G
ENST00000590755.6:c.427A>G	ENSP00000476667.1:n.427A>G
ENST00000593163.5:n.765A>G
ENST00000609145.5:c.33A>G	ENSP00000476514.1:p.Lys11=
NM_000285.3:c.600A>G	NP_000276.2:p.Lys200=
NM_001166056.1:c.548+14035A>G	NP_001159528.1:n.548+14035A>G
NM_001166057.1:c.408A>G	NP_001159529.1:p.Lys136=
NM_000285.4:c.600A>G MANE Select	NP_000276.2:p.Lys200=
NM_001166056.2:c.548+14035A>G	NP_001159528.1:n.548+14035A>G
NM_001166057.2:c.408A>G	NP_001159529.1:p.Lys136=