Canonical Allele Identifier: CA2241805443
Gene: DPEP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614682C= , CM000678.2:g.89614682C= GRCh38
NC_000016.9:g.89681090C= , CM000678.1:g.89681090C= GRCh37
NC_000016.8:g.88208591C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+963C= MANE Select ENSP00000508584.1:n.-107+963C=
ENST00000421184.5:c.-107+1278C= ENSP00000397313.1:n.-107+1278C=
ENST00000564281.5:n.47+963C=
ENST00000565249.5:n.171+963C=
ENST00000570029.5:c.-107+1278C= ENSP00000455916.1:n.-107+1278C=
NM_001128141.2:c.-107+1278C= NP_001121613.1:n.-107+1278C=
XM_005256285.3:c.-107+963C= XP_005256342.1:n.-107+963C=
XM_011522926.1:c.-107+963C= XP_011521228.1:n.-107+963C=
XM_005256285.5:c.-107+963C= XP_005256342.1:n.-107+963C=
NM_001128141.3:c.-107+1278C= NP_001121613.1:n.-107+1278C=
NM_001389466.1:c.-107+963C= MANE Select NP_001376395.1:n.-107+963C=
NM_001389470.1:c.-107+963C= NP_001376399.1:n.-107+963C=