Canonical Allele Identifier: CA980450307
Gene: DPEP1 HGNC NCBI

Linked Data

dbSNP Id: rs2059367118

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614838dup , CM000678.2:g.89614838dup GRCh38
NC_000016.9:g.89681246dup , CM000678.1:g.89681246dup GRCh37
NC_000016.8:g.88208747dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+1119dup MANE Select ENSP00000508584.1:n.-107+1119dup
ENST00000421184.5:c.-107+1434dup ENSP00000397313.1:n.-107+1434dup
ENST00000564281.5:n.47+1119dup
ENST00000565249.5:n.171+1119dup
ENST00000570029.5:c.-107+1434dup ENSP00000455916.1:n.-107+1434dup
NM_001128141.2:c.-107+1434dup NP_001121613.1:n.-107+1434dup
XM_005256285.3:c.-107+1119dup XP_005256342.1:n.-107+1119dup
XM_011522926.1:c.-107+1119dup XP_011521228.1:n.-107+1119dup
XM_005256285.5:c.-107+1119dup XP_005256342.1:n.-107+1119dup
NM_001128141.3:c.-107+1434dup NP_001121613.1:n.-107+1434dup
NM_001389466.1:c.-107+1119dup MANE Select NP_001376395.1:n.-107+1119dup
NM_001389470.1:c.-107+1119dup NP_001376399.1:n.-107+1119dup