Canonical Allele Identifier: CA881604784

Gene: PEPD

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33398094G>C , CM000681.2:g.33398094G>C	GRCh38
NC_000019.9:g.33889000G>C , CM000681.1:g.33889000G>C	GRCh37
NC_000019.8:g.38580840G>C	NCBI36
NG_013358.1:g.128800C>G
NG_013358.2:g.128800C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.968-1939C>G	ENSP00000468516.4:n.968-1939C>G
ENST00000651901.2:c.967+3627C>G	ENSP00000498922.2:n.967+3627C>G
ENST00000698359.1:c.922+3627C>G	ENSP00000513682.1:n.922+3627C>G
ENST00000698360.1:c.1018+3627C>G	ENSP00000513683.1:n.1018+3627C>G
ENST00000698361.1:c.967+3627C>G	ENSP00000513684.1:n.967+3627C>G
ENST00000698362.1:c.967+3627C>G	ENSP00000513685.1:n.967+3627C>G
ENST00000698426.1:c.646+3627C>G	ENSP00000513713.1:n.646+3627C>G
ENST00000698427.1:c.1009+3627C>G	ENSP00000513714.1:n.1009+3627C>G
ENST00000698428.1:c.646+3627C>G	ENSP00000513715.1:n.646+3627C>G
ENST00000698429.1:n.850+3627C>G
ENST00000698430.1:c.1217+3627C>G
ENST00000698431.1:c.704+3627C>G	ENSP00000513717.1:n.704+3627C>G
ENST00000698432.1:c.776+3627C>G
ENST00000698433.1:n.429+3627C>G
ENST00000698434.1:n.454+3627C>G
ENST00000244137.12:c.967+3627C>G MANE Select	ENSP00000244137.5:n.967+3627C>G
ENST00000588328.6:c.957-1939C>G
ENST00000590731.6:n.642+3627C>G
ENST00000651901.1:c.963+3627C>G
ENST00000244137.11:c.967+3627C>G	ENSP00000244137.5:n.967+3627C>G
ENST00000397032.8:c.844+3627C>G	ENSP00000380226.3:n.844+3627C>G
ENST00000436370.7:c.775+3627C>G	ENSP00000391890.2:n.775+3627C>G
ENST00000588328.5:c.459-1939C>G
NM_000285.3:c.967+3627C>G	NP_000276.2:n.967+3627C>G
NM_001166056.1:c.844+3627C>G	NP_001159528.1:n.844+3627C>G
NM_001166057.1:c.775+3627C>G	NP_001159529.1:n.775+3627C>G
NM_000285.4:c.967+3627C>G MANE Select	NP_000276.2:n.967+3627C>G
NM_001166056.2:c.844+3627C>G	NP_001159528.1:n.844+3627C>G
NM_001166057.2:c.775+3627C>G	NP_001159529.1:n.775+3627C>G