Canonical Allele Identifier: CA2241805547
Gene: DPEP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614790G= , CM000678.2:g.89614790G= GRCh38
NC_000016.9:g.89681198G= , CM000678.1:g.89681198G= GRCh37
NC_000016.8:g.88208699G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+1071G= MANE Select ENSP00000508584.1:n.-107+1071G=
ENST00000421184.5:c.-107+1386G= ENSP00000397313.1:n.-107+1386G=
ENST00000564281.5:n.47+1071G=
ENST00000565249.5:n.171+1071G=
ENST00000570029.5:c.-107+1386G= ENSP00000455916.1:n.-107+1386G=
NM_001128141.2:c.-107+1386G= NP_001121613.1:n.-107+1386G=
XM_005256285.3:c.-107+1071G= XP_005256342.1:n.-107+1071G=
XM_011522926.1:c.-107+1071G= XP_011521228.1:n.-107+1071G=
XM_005256285.5:c.-107+1071G= XP_005256342.1:n.-107+1071G=
NM_001128141.3:c.-107+1386G= NP_001121613.1:n.-107+1386G=
NM_001389466.1:c.-107+1071G= MANE Select NP_001376395.1:n.-107+1071G=
NM_001389470.1:c.-107+1071G= NP_001376399.1:n.-107+1071G=