Canonical Allele Identifier: CA725750372
Gene: DPEP1 HGNC NCBI

Linked Data

dbSNP Id: rs1343753147
gnomAD v3: 16-89614703-G-A
gnomAD v4: 16-89614703-G-A
MyVariant Identifiers: chr16:g.89681111G>A (hg19) chr16:g.89614703G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89614703G>A , CM000678.2:g.89614703G>A GRCh38
NC_000016.9:g.89681111G>A , CM000678.1:g.89681111G>A GRCh37
NC_000016.8:g.88208612G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690203.1:c.-107+984G>A MANE Select ENSP00000508584.1:n.-107+984G>A
ENST00000421184.5:c.-107+1299G>A ENSP00000397313.1:n.-107+1299G>A
ENST00000564281.5:n.47+984G>A
ENST00000565249.5:n.171+984G>A
ENST00000570029.5:c.-107+1299G>A ENSP00000455916.1:n.-107+1299G>A
NM_001128141.2:c.-107+1299G>A NP_001121613.1:n.-107+1299G>A
XM_005256285.3:c.-107+984G>A XP_005256342.1:n.-107+984G>A
XM_011522926.1:c.-107+984G>A XP_011521228.1:n.-107+984G>A
XM_005256285.5:c.-107+984G>A XP_005256342.1:n.-107+984G>A
NM_001128141.3:c.-107+1299G>A NP_001121613.1:n.-107+1299G>A
NM_001389466.1:c.-107+984G>A MANE Select NP_001376395.1:n.-107+984G>A
NM_001389470.1:c.-107+984G>A NP_001376399.1:n.-107+984G>A
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