Canonical Allele Identifier: CA2332706023
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33401641_33401645delinsGTTCC , CM000681.2:g.33401641_33401645delinsGTTCC GRCh38
NC_000019.9:g.33892547_33892551delinsGTTCC , CM000681.1:g.33892547_33892551delinsGTTCC GRCh37
NC_000019.8:g.38584387_38584391delinsGTTCC NCBI36
NG_013358.1:g.125249_125253delinsGGAAC
NG_013358.2:g.125249_125253delinsGGAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000588328.7:c.967+76_967+80delinsGGAAC ENSP00000468516.4:n.967+76_967+80delinsGGAAC
ENST00000651901.2:c.967+76_967+80delinsGGAAC ENSP00000498922.2:n.967+76_967+80delinsGGAAC
ENST00000698359.1:c.922+76_922+80delinsGGAAC ENSP00000513682.1:n.922+76_922+80delinsGGAAC
ENST00000698360.1:c.1018+76_1018+80delinsGGAAC ENSP00000513683.1:n.1018+76_1018+80delinsGGAAC
ENST00000698361.1:c.967+76_967+80delinsGGAAC ENSP00000513684.1:n.967+76_967+80delinsGGAAC
ENST00000698362.1:c.967+76_967+80delinsGGAAC ENSP00000513685.1:n.967+76_967+80delinsGGAAC
ENST00000698363.1:n.1030+76_1030+80delinsGGAAC
ENST00000698364.1:n.1030+76_1030+80delinsGGAAC
ENST00000698365.1:n.1106_1110delinsGGAAC
ENST00000698426.1:c.646+76_646+80delinsGGAAC ENSP00000513713.1:n.646+76_646+80delinsGGAAC
ENST00000698427.1:c.1009+76_1009+80delinsGGAAC ENSP00000513714.1:n.1009+76_1009+80delinsGGAAC
ENST00000698428.1:c.646+76_646+80delinsGGAAC ENSP00000513715.1:n.646+76_646+80delinsGGAAC
ENST00000698429.1:n.850+76_850+80delinsGGAAC
ENST00000698430.1:c.1217+76_1217+80delinsGGAAC
ENST00000698431.1:c.704+76_704+80delinsGGAAC ENSP00000513717.1:n.704+76_704+80delinsGGAAC
ENST00000698432.1:c.776+76_776+80delinsGGAAC
ENST00000698433.1:n.429+76_429+80delinsGGAAC
ENST00000698434.1:n.454+76_454+80delinsGGAAC
ENST00000244137.12:c.967+76_967+80delinsGGAAC MANE Select ENSP00000244137.5:n.967+76_967+80delinsGGAAC
ENST00000588328.6:c.956+76_956+80delinsGGAAC
ENST00000590731.6:n.642+76_642+80delinsGGAAC
ENST00000651901.1:c.963+76_963+80delinsGGAAC
ENST00000244137.11:c.967+76_967+80delinsGGAAC ENSP00000244137.5:n.967+76_967+80delinsGGAAC
ENST00000397032.8:c.844+76_844+80delinsGGAAC ENSP00000380226.3:n.844+76_844+80delinsGGAAC
ENST00000436370.7:c.775+76_775+80delinsGGAAC ENSP00000391890.2:n.775+76_775+80delinsGGAAC
ENST00000588328.5:c.458+76_458+80delinsGGAAC
NM_000285.3:c.967+76_967+80delinsGGAAC NP_000276.2:n.967+76_967+80delinsGGAAC
NM_001166056.1:c.844+76_844+80delinsGGAAC NP_001159528.1:n.844+76_844+80delinsGGAAC
NM_001166057.1:c.775+76_775+80delinsGGAAC NP_001159529.1:n.775+76_775+80delinsGGAAC
NM_000285.4:c.967+76_967+80delinsGGAAC MANE Select NP_000276.2:n.967+76_967+80delinsGGAAC
NM_001166056.2:c.844+76_844+80delinsGGAAC NP_001159528.1:n.844+76_844+80delinsGGAAC
NM_001166057.2:c.775+76_775+80delinsGGAAC NP_001159529.1:n.775+76_775+80delinsGGAAC