Canonical Allele Identifier: CA2332709286

Gene: PEPD

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33408159G>C , CM000681.2:g.33408159G>C	GRCh38
NC_000019.9:g.33899065G>C , CM000681.1:g.33899065G>C	GRCh37
NC_000019.8:g.38590905G>C	NCBI36
NG_013358.1:g.118735C>G
NG_013358.2:g.118735C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.818+3513C>G	ENSP00000468516.4:n.818+3513C>G
ENST00000651901.2:c.818+3513C>G	ENSP00000498922.2:n.818+3513C>G
ENST00000698359.1:c.773+3513C>G	ENSP00000513682.1:n.773+3513C>G
ENST00000698360.1:c.869+3513C>G	ENSP00000513683.1:n.869+3513C>G
ENST00000698361.1:c.818+3513C>G	ENSP00000513684.1:n.818+3513C>G
ENST00000698362.1:c.818+3513C>G	ENSP00000513685.1:n.818+3513C>G
ENST00000698363.1:n.881+3513C>G
ENST00000698364.1:n.881+3513C>G
ENST00000698365.1:n.881+3513C>G
ENST00000698426.1:c.497+3513C>G	ENSP00000513713.1:n.497+3513C>G
ENST00000698427.1:c.860+3513C>G	ENSP00000513714.1:n.860+3513C>G
ENST00000698428.1:c.497+3513C>G	ENSP00000513715.1:n.497+3513C>G
ENST00000698429.1:n.701+3513C>G
ENST00000698430.1:c.1068+3513C>G
ENST00000698431.1:c.555+3513C>G	ENSP00000513717.1:n.555+3513C>G
ENST00000698432.1:c.627+3513C>G
ENST00000698433.1:n.280+3513C>G
ENST00000698434.1:n.305+3513C>G
ENST00000698435.1:c.506+3513C>G	ENSP00000513719.1:n.506+3513C>G
ENST00000244137.12:c.818+3513C>G MANE Select	ENSP00000244137.5:n.818+3513C>G
ENST00000588328.6:c.807+3513C>G
ENST00000590731.6:n.493+3513C>G
ENST00000651901.1:c.814+3513C>G
ENST00000244137.11:c.818+3513C>G	ENSP00000244137.5:n.818+3513C>G
ENST00000397032.8:c.695+3513C>G	ENSP00000380226.3:n.695+3513C>G
ENST00000436370.7:c.626+3513C>G	ENSP00000391890.2:n.626+3513C>G
ENST00000588328.5:c.309+3513C>G
ENST00000588719.5:n.453+3513C>G
ENST00000590731.5:n.493+3513C>G
ENST00000593163.5:n.983+3513C>G
ENST00000609145.5:c.251+3513C>G	ENSP00000476514.1:n.251+3513C>G
NM_000285.3:c.818+3513C>G	NP_000276.2:n.818+3513C>G
NM_001166056.1:c.695+3513C>G	NP_001159528.1:n.695+3513C>G
NM_001166057.1:c.626+3513C>G	NP_001159529.1:n.626+3513C>G
NM_000285.4:c.818+3513C>G MANE Select	NP_000276.2:n.818+3513C>G
NM_001166056.2:c.695+3513C>G	NP_001159528.1:n.695+3513C>G
NM_001166057.2:c.626+3513C>G	NP_001159529.1:n.626+3513C>G