Canonical Allele Identifier: CA2553212990

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401587_33401588insCCT , CM000681.2:g.33401587_33401588insCCT	GRCh38
NC_000019.9:g.33892493_33892494insCCT , CM000681.1:g.33892493_33892494insCCT	GRCh37
NC_000019.8:g.38584333_38584334insCCT	NCBI36
NG_013358.1:g.125306_125307insAGG
NG_013358.2:g.125306_125307insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.967+133_967+134insAGG	ENSP00000468516.4:n.967+133_967+134insAGG
ENST00000651901.2:c.967+133_967+134insAGG	ENSP00000498922.2:n.967+133_967+134insAGG
ENST00000698359.1:c.922+133_922+134insAGG	ENSP00000513682.1:n.922+133_922+134insAGG
ENST00000698360.1:c.1018+133_1018+134insAGG	ENSP00000513683.1:n.1018+133_1018+134insAGG
ENST00000698361.1:c.967+133_967+134insAGG	ENSP00000513684.1:n.967+133_967+134insAGG
ENST00000698362.1:c.967+133_967+134insAGG	ENSP00000513685.1:n.967+133_967+134insAGG
ENST00000698363.1:n.1030+133_1030+134insAGG
ENST00000698364.1:n.1030+133_1030+134insAGG
ENST00000698365.1:n.1163_1164insAGG
ENST00000698426.1:c.646+133_646+134insAGG	ENSP00000513713.1:n.646+133_646+134insAGG
ENST00000698427.1:c.1009+133_1009+134insAGG	ENSP00000513714.1:n.1009+133_1009+134insAGG
ENST00000698428.1:c.646+133_646+134insAGG	ENSP00000513715.1:n.646+133_646+134insAGG
ENST00000698429.1:n.850+133_850+134insAGG
ENST00000698430.1:c.1217+133_1217+134insAGG
ENST00000698431.1:c.704+133_704+134insAGG	ENSP00000513717.1:n.704+133_704+134insAGG
ENST00000698432.1:c.776+133_776+134insAGG
ENST00000698433.1:n.429+133_429+134insAGG
ENST00000698434.1:n.454+133_454+134insAGG
ENST00000244137.12:c.967+133_967+134insAGG MANE Select	ENSP00000244137.5:n.967+133_967+134insAGG
ENST00000588328.6:c.956+133_956+134insAGG
ENST00000590731.6:n.642+133_642+134insAGG
ENST00000651901.1:c.963+133_963+134insAGG
ENST00000244137.11:c.967+133_967+134insAGG	ENSP00000244137.5:n.967+133_967+134insAGG
ENST00000397032.8:c.844+133_844+134insAGG	ENSP00000380226.3:n.844+133_844+134insAGG
ENST00000436370.7:c.775+133_775+134insAGG	ENSP00000391890.2:n.775+133_775+134insAGG
ENST00000588328.5:c.458+133_458+134insAGG
NM_000285.3:c.967+133_967+134insAGG	NP_000276.2:n.967+133_967+134insAGG
NM_001166056.1:c.844+133_844+134insAGG	NP_001159528.1:n.844+133_844+134insAGG
NM_001166057.1:c.775+133_775+134insAGG	NP_001159529.1:n.775+133_775+134insAGG
NM_000285.4:c.967+133_967+134insAGG MANE Select	NP_000276.2:n.967+133_967+134insAGG
NM_001166056.2:c.844+133_844+134insAGG	NP_001159528.1:n.844+133_844+134insAGG
NM_001166057.2:c.775+133_775+134insAGG	NP_001159529.1:n.775+133_775+134insAGG