Canonical Allele Identifier: CA2241805469
Gene: DPEP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614707A= , CM000678.2:g.89614707A= GRCh38
NC_000016.9:g.89681115A= , CM000678.1:g.89681115A= GRCh37
NC_000016.8:g.88208616A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+988A= MANE Select ENSP00000508584.1:n.-107+988A=
ENST00000421184.5:c.-107+1303A= ENSP00000397313.1:n.-107+1303A=
ENST00000564281.5:n.47+988A=
ENST00000565249.5:n.171+988A=
ENST00000570029.5:c.-107+1303A= ENSP00000455916.1:n.-107+1303A=
NM_001128141.2:c.-107+1303A= NP_001121613.1:n.-107+1303A=
XM_005256285.3:c.-107+988A= XP_005256342.1:n.-107+988A=
XM_011522926.1:c.-107+988A= XP_011521228.1:n.-107+988A=
XM_005256285.5:c.-107+988A= XP_005256342.1:n.-107+988A=
NM_001128141.3:c.-107+1303A= NP_001121613.1:n.-107+1303A=
NM_001389466.1:c.-107+988A= MANE Select NP_001376395.1:n.-107+988A=
NM_001389470.1:c.-107+988A= NP_001376399.1:n.-107+988A=
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