Canonical Allele Identifier: CA169613987
Gene: DPP6 HGNC NCBI

Linked Data

dbSNP Id: rs1041598022
gnomAD v3: 7-153861502-G-A
gnomAD v4: 7-153861502-G-A
MyVariant Identifiers: chr7:g.153558587G>A (hg19) chr7:g.153861502G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.153861502G>A , CM000669.2:g.153861502G>A GRCh38
NC_000007.13:g.153558587G>A , CM000669.1:g.153558587G>A GRCh37
NC_000007.12:g.153189520G>A NCBI36
NG_033878.2:g.118517G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706130.1:c.60+112494G>A ENSP00000516215.1:n.60+112494G>A
NM_001364497.1:c.60+112494G>A NP_001351426.1:n.60+112494G>A
NM_001364498.1:c.60+112494G>A NP_001351427.1:n.60+112494G>A
NM_001364499.1:c.60+112494G>A NP_001351428.1:n.60+112494G>A
NM_001364500.1:c.60+112494G>A NP_001351429.1:n.60+112494G>A
XR_001745002.1:n.3345+2879G>A
NM_001364497.2:c.60+112494G>A NP_001351426.1:n.60+112494G>A
NM_001364498.2:c.60+112494G>A NP_001351427.1:n.60+112494G>A
NM_001364499.2:c.60+112494G>A NP_001351428.1:n.60+112494G>A
NM_001364500.2:c.60+112494G>A NP_001351429.1:n.60+112494G>A
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