Canonical Allele Identifier: CA169258129
Gene: DPP6 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.154801156T>G
GRCh37 chr7:g.154592866T>G
gnomAD v2:
7:154592866 T / G
gnomAD v3:
7:154801156 T / G
gnomAD v4:
chr7-154801156-T-G
Joint Max Group AF 0.07345783 (NFE)
Genomes Max Group AF 0.07345783 (NFE)
ClinVar RCV:
RCV001648975
ClinVar Variation:
1244767
dbSNP:
71534169
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.154801156T>G , CM000669.2:g.154801156T>G GRCh38
NC_000007.13:g.154592866T>G , CM000669.1:g.154592866T>G GRCh37
NC_000007.12:g.154223799T>G NCBI36
NG_033878.1:g.918823T>G
NG_033878.2:g.1058171T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706130.1:c.1117-199T>G ENSP00000516215.1:n.1117-199T>G
ENST00000706151.1:c.325-199T>G ENSP00000516234.1:n.325-199T>G
ENST00000706153.1:n.946-199T>G
ENST00000706154.1:n.584-199T>G
ENST00000706155.1:n.731-199T>G
ENST00000377770.8:c.1300-199T>G MANE Select ENSP00000367001.3:n.1300-199T>G
ENST00000332007.7:c.1114-199T>G ENSP00000328226.3:n.1114-199T>G
ENST00000377770.7:c.1300-199T>G ENSP00000367001.3:n.1300-199T>G
ENST00000404039.5:c.1108-199T>G ENSP00000385578.1:n.1108-199T>G
ENST00000427557.1:c.979-199T>G ENSP00000397303.1:n.979-199T>G
ENST00000471100.5:n.446-199T>G
NM_001039350.2:c.1108-199T>G NP_001034439.1:n.1108-199T>G
NM_001290252.1:c.979-199T>G NP_001277181.1:n.979-199T>G
NM_001936.4:c.1114-199T>G NP_001927.3:n.1114-199T>G
NM_130797.3:c.1300-199T>G NP_570629.2:n.1300-199T>G
XM_011515865.1:c.1108-199T>G XP_011514167.1:n.1108-199T>G
XM_011515866.1:c.676-199T>G XP_011514168.1:n.676-199T>G
NM_001364497.1:c.1117-199T>G NP_001351426.1:n.1117-199T>G
NM_001364498.1:c.1117-199T>G NP_001351427.1:n.1117-199T>G
NM_001364499.1:c.1117-199T>G NP_001351428.1:n.1117-199T>G
NM_001364500.1:c.1117-199T>G NP_001351429.1:n.1117-199T>G
NR_157195.1:n.1750-199T>G
NR_157196.1:n.1450-199T>G
XM_017011812.2:c.676-199T>G XP_016867301.1:n.676-199T>G
NM_130797.4:c.1300-199T>G MANE Select NP_570629.2:n.1300-199T>G
NM_001039350.3:c.1108-199T>G NP_001034439.1:n.1108-199T>G
NM_001290252.2:c.979-199T>G NP_001277181.1:n.979-199T>G
NM_001364497.2:c.1117-199T>G NP_001351426.1:n.1117-199T>G
NM_001364498.2:c.1117-199T>G NP_001351427.1:n.1117-199T>G
NM_001364499.2:c.1117-199T>G NP_001351428.1:n.1117-199T>G
NM_001364500.2:c.1117-199T>G NP_001351429.1:n.1117-199T>G
NM_001936.5:c.1114-199T>G NP_001927.3:n.1114-199T>G
NR_157196.2:n.1450-199T>G
NR_157195.2:n.1750-199T>G
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