Canonical Allele Identifier: CA995299809
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs1968492734

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33401650_33401651insCAA , CM000681.2:g.33401650_33401651insCAA GRCh38
NC_000019.9:g.33892556_33892557insCAA , CM000681.1:g.33892556_33892557insCAA GRCh37
NC_000019.8:g.38584396_38584397insCAA NCBI36
NG_013358.1:g.125244_125245insTGT
NG_013358.2:g.125244_125245insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000588328.7:c.967+71_967+72insTGT ENSP00000468516.4:n.967+71_967+72insTGT
ENST00000651901.2:c.967+71_967+72insTGT ENSP00000498922.2:n.967+71_967+72insTGT
ENST00000698359.1:c.922+71_922+72insTGT ENSP00000513682.1:n.922+71_922+72insTGT
ENST00000698360.1:c.1018+71_1018+72insTGT ENSP00000513683.1:n.1018+71_1018+72insTGT
ENST00000698361.1:c.967+71_967+72insTGT ENSP00000513684.1:n.967+71_967+72insTGT
ENST00000698362.1:c.967+71_967+72insTGT ENSP00000513685.1:n.967+71_967+72insTGT
ENST00000698363.1:n.1030+71_1030+72insTGT
ENST00000698364.1:n.1030+71_1030+72insTGT
ENST00000698365.1:n.1101_1102insTGT
ENST00000698426.1:c.646+71_646+72insTGT ENSP00000513713.1:n.646+71_646+72insTGT
ENST00000698427.1:c.1009+71_1009+72insTGT ENSP00000513714.1:n.1009+71_1009+72insTGT
ENST00000698428.1:c.646+71_646+72insTGT ENSP00000513715.1:n.646+71_646+72insTGT
ENST00000698429.1:n.850+71_850+72insTGT
ENST00000698430.1:c.1217+71_1217+72insTGT
ENST00000698431.1:c.704+71_704+72insTGT ENSP00000513717.1:n.704+71_704+72insTGT
ENST00000698432.1:c.776+71_776+72insTGT
ENST00000698433.1:n.429+71_429+72insTGT
ENST00000698434.1:n.454+71_454+72insTGT
ENST00000244137.12:c.967+71_967+72insTGT MANE Select ENSP00000244137.5:n.967+71_967+72insTGT
ENST00000588328.6:c.956+71_956+72insTGT
ENST00000590731.6:n.642+71_642+72insTGT
ENST00000651901.1:c.963+71_963+72insTGT
ENST00000244137.11:c.967+71_967+72insTGT ENSP00000244137.5:n.967+71_967+72insTGT
ENST00000397032.8:c.844+71_844+72insTGT ENSP00000380226.3:n.844+71_844+72insTGT
ENST00000436370.7:c.775+71_775+72insTGT ENSP00000391890.2:n.775+71_775+72insTGT
ENST00000588328.5:c.458+71_458+72insTGT
NM_000285.3:c.967+71_967+72insTGT NP_000276.2:n.967+71_967+72insTGT
NM_001166056.1:c.844+71_844+72insTGT NP_001159528.1:n.844+71_844+72insTGT
NM_001166057.1:c.775+71_775+72insTGT NP_001159529.1:n.775+71_775+72insTGT
NM_000285.4:c.967+71_967+72insTGT MANE Select NP_000276.2:n.967+71_967+72insTGT
NM_001166056.2:c.844+71_844+72insTGT NP_001159528.1:n.844+71_844+72insTGT
NM_001166057.2:c.775+71_775+72insTGT NP_001159529.1:n.775+71_775+72insTGT