Canonical Allele Identifier: CA2241805489
Gene: DPEP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614727G= , CM000678.2:g.89614727G= GRCh38
NC_000016.9:g.89681135G= , CM000678.1:g.89681135G= GRCh37
NC_000016.8:g.88208636G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+1008G= MANE Select ENSP00000508584.1:n.-107+1008G=
ENST00000421184.5:c.-107+1323G= ENSP00000397313.1:n.-107+1323G=
ENST00000564281.5:n.47+1008G=
ENST00000565249.5:n.171+1008G=
ENST00000570029.5:c.-107+1323G= ENSP00000455916.1:n.-107+1323G=
NM_001128141.2:c.-107+1323G= NP_001121613.1:n.-107+1323G=
XM_005256285.3:c.-107+1008G= XP_005256342.1:n.-107+1008G=
XM_011522926.1:c.-107+1008G= XP_011521228.1:n.-107+1008G=
XM_005256285.5:c.-107+1008G= XP_005256342.1:n.-107+1008G=
NM_001128141.3:c.-107+1323G= NP_001121613.1:n.-107+1323G=
NM_001389466.1:c.-107+1008G= MANE Select NP_001376395.1:n.-107+1008G=
NM_001389470.1:c.-107+1008G= NP_001376399.1:n.-107+1008G=