Canonical Allele Identifier: CA1932025
Gene: DPP4 HGNC NCBI

Linked Data

dbSNP Id: rs41268649
ExAC: 2:162865133 C / T
gnomAD v2: 2-162865133-C-T
gnomAD v3: 2-162008623-C-T
gnomAD v4: 2-162008623-C-T
MyVariant Identifiers: chr2:g.162865133C>T (hg19) chr2:g.162008623C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162008623C>T , CM000664.2:g.162008623C>T GRCh38
NC_000002.11:g.162865133C>T , CM000664.1:g.162865133C>T GRCh37
NC_000002.10:g.162573379C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360534.8:c.1926G>A MANE Select ENSP00000353731.3:p.Ser642=
ENST00000416189.6:c.*1620G>A ENSP00000401359.2:n.*1620G>A
ENST00000494507.2:c.*1620G>A ENSP00000503735.1:n.*1620G>A
ENST00000676479.1:c.*1929G>A ENSP00000504273.1:n.*1929G>A
ENST00000676624.1:c.*1673G>A ENSP00000503481.1:n.*1673G>A
ENST00000676768.1:c.1926G>A ENSP00000503008.1:p.Ser642=
ENST00000676810.1:c.1923G>A ENSP00000503161.1:p.Ser641=
ENST00000676996.1:n.2080G>A
ENST00000677015.1:n.1585G>A
ENST00000677212.1:n.2107G>A
ENST00000678522.1:n.2160G>A
ENST00000678566.1:c.*1266G>A ENSP00000502931.1:n.*1266G>A
ENST00000678583.1:n.7132G>A
ENST00000678668.1:c.1050G>A ENSP00000504418.1:p.Ser350=
ENST00000678740.1:n.2157G>A
ENST00000679104.1:c.*1620G>A ENSP00000504157.1:n.*1620G>A
ENST00000360534.7:c.1926G>A ENSP00000353731.3:p.Ser642=
ENST00000434918.6:c.*1645G>A ENSP00000402259.2:n.*1645G>A
ENST00000490286.5:n.1920G>A
ENST00000491591.5:n.696G>A
ENST00000494507.1:n.356G>A
NM_001935.3:c.1926G>A NP_001926.2:p.Ser642=
XM_005246371.2:c.1923G>A XP_005246428.1:p.Ser641=
XM_005246371.3:c.1923G>A XP_005246428.1:p.Ser641=
NM_001935.4:c.1926G>A MANE Select NP_001926.2:p.Ser642=
NM_001379604.1:c.1923G>A NP_001366533.1:p.Ser641=
NM_001379605.1:c.1920G>A NP_001366534.1:p.Ser640=
NM_001379606.1:c.1872G>A NP_001366535.1:p.Ser624=
NR_166822.1:n.2392G>A
NR_166823.1:n.2400G>A
NR_166824.1:n.2158G>A
NR_166825.1:n.2107G>A
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