Canonical Allele Identifier: CA2241805289
Gene: DPEP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614533_89614541delinsGCCTGTAAT , CM000678.2:g.89614533_89614541delinsGCCTGTAAT GRCh38
NC_000016.9:g.89680941_89680949delinsGCCTGTAAT , CM000678.1:g.89680941_89680949delinsGCCTGTAAT GRCh37
NC_000016.8:g.88208442_88208450delinsGCCTGTAAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+814_-107+822delinsGCCTGTAAT MANE Select ENSP00000508584.1:n.-107+814_-107+822delinsGCCTGTAAT
ENST00000421184.5:c.-107+1129_-107+1137delinsGCCTGTAAT ENSP00000397313.1:n.-107+1129_-107+1137delinsGCCTGTAAT
ENST00000564281.5:n.47+814_47+822delinsGCCTGTAAT
ENST00000565249.5:n.171+814_171+822delinsGCCTGTAAT
ENST00000570029.5:c.-107+1129_-107+1137delinsGCCTGTAAT ENSP00000455916.1:n.-107+1129_-107+1137delinsGCCTGTAAT
NM_001128141.2:c.-107+1129_-107+1137delinsGCCTGTAAT NP_001121613.1:n.-107+1129_-107+1137delinsGCCTGTAAT
XM_005256285.3:c.-107+814_-107+822delinsGCCTGTAAT XP_005256342.1:n.-107+814_-107+822delinsGCCTGTAAT
XM_011522926.1:c.-107+814_-107+822delinsGCCTGTAAT XP_011521228.1:n.-107+814_-107+822delinsGCCTGTAAT
XM_005256285.5:c.-107+814_-107+822delinsGCCTGTAAT XP_005256342.1:n.-107+814_-107+822delinsGCCTGTAAT
NM_001128141.3:c.-107+1129_-107+1137delinsGCCTGTAAT NP_001121613.1:n.-107+1129_-107+1137delinsGCCTGTAAT
NM_001389466.1:c.-107+814_-107+822delinsGCCTGTAAT MANE Select NP_001376395.1:n.-107+814_-107+822delinsGCCTGTAAT
NM_001389470.1:c.-107+814_-107+822delinsGCCTGTAAT NP_001376399.1:n.-107+814_-107+822delinsGCCTGTAAT