Canonical Allele Identifier: CA725750549
Gene: DPEP1 HGNC NCBI

Linked Data

dbSNP Id: rs114464690
MyVariant Identifiers: chr16:g.89681319C>A (hg19) chr16:g.89614911C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614911C>A , CM000678.2:g.89614911C>A GRCh38
NC_000016.9:g.89681319C>A , CM000678.1:g.89681319C>A GRCh37
NC_000016.8:g.88208820C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+1192C>A MANE Select ENSP00000508584.1:n.-107+1192C>A
ENST00000421184.5:c.-107+1507C>A ENSP00000397313.1:n.-107+1507C>A
ENST00000564281.5:n.47+1192C>A
ENST00000565249.5:n.171+1192C>A
ENST00000570029.5:c.-107+1507C>A ENSP00000455916.1:n.-107+1507C>A
NM_001128141.2:c.-107+1507C>A NP_001121613.1:n.-107+1507C>A
XM_005256285.3:c.-107+1192C>A XP_005256342.1:n.-107+1192C>A
XM_011522926.1:c.-107+1192C>A XP_011521228.1:n.-107+1192C>A
XM_005256285.5:c.-107+1192C>A XP_005256342.1:n.-107+1192C>A
NM_001128141.3:c.-107+1507C>A NP_001121613.1:n.-107+1507C>A
NM_001389466.1:c.-107+1192C>A MANE Select NP_001376395.1:n.-107+1192C>A
NM_001389470.1:c.-107+1192C>A NP_001376399.1:n.-107+1192C>A
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