Canonical Allele Identifier: CA2241805504
Gene: DPEP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614753_89614758delinsCCACTG , CM000678.2:g.89614753_89614758delinsCCACTG GRCh38
NC_000016.9:g.89681161_89681166delinsCCACTG , CM000678.1:g.89681161_89681166delinsCCACTG GRCh37
NC_000016.8:g.88208662_88208667delinsCCACTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+1034_-107+1039delinsCCACTG MANE Select ENSP00000508584.1:n.-107+1034_-107+1039delinsCCACTG
ENST00000421184.5:c.-107+1349_-107+1354delinsCCACTG ENSP00000397313.1:n.-107+1349_-107+1354delinsCCACTG
ENST00000564281.5:n.47+1034_47+1039delinsCCACTG
ENST00000565249.5:n.171+1034_171+1039delinsCCACTG
ENST00000570029.5:c.-107+1349_-107+1354delinsCCACTG ENSP00000455916.1:n.-107+1349_-107+1354delinsCCACTG
NM_001128141.2:c.-107+1349_-107+1354delinsCCACTG NP_001121613.1:n.-107+1349_-107+1354delinsCCACTG
XM_005256285.3:c.-107+1034_-107+1039delinsCCACTG XP_005256342.1:n.-107+1034_-107+1039delinsCCACTG
XM_011522926.1:c.-107+1034_-107+1039delinsCCACTG XP_011521228.1:n.-107+1034_-107+1039delinsCCACTG
XM_005256285.5:c.-107+1034_-107+1039delinsCCACTG XP_005256342.1:n.-107+1034_-107+1039delinsCCACTG
NM_001128141.3:c.-107+1349_-107+1354delinsCCACTG NP_001121613.1:n.-107+1349_-107+1354delinsCCACTG
NM_001389466.1:c.-107+1034_-107+1039delinsCCACTG MANE Select NP_001376395.1:n.-107+1034_-107+1039delinsCCACTG
NM_001389470.1:c.-107+1034_-107+1039delinsCCACTG NP_001376399.1:n.-107+1034_-107+1039delinsCCACTG