Canonical Allele Identifier: CA1303036927
Gene: DPP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162044379C>G , CM000664.2:g.162044379C>G GRCh38
NC_000002.11:g.162900889C>G , CM000664.1:g.162900889C>G GRCh37
NC_000002.10:g.162609135C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360534.8:c.366+1153G>C MANE Select ENSP00000353731.3:n.366+1153G>C
ENST00000416189.6:c.*113+1153G>C ENSP00000401359.2:n.*113+1153G>C
ENST00000461836.6:n.951+1153G>C
ENST00000494507.2:c.*113+1153G>C ENSP00000503735.1:n.*113+1153G>C
ENST00000676479.1:c.*369+1153G>C ENSP00000504273.1:n.*369+1153G>C
ENST00000676624.1:c.*113+1153G>C ENSP00000503481.1:n.*113+1153G>C
ENST00000676768.1:c.366+1153G>C ENSP00000503008.1:n.366+1153G>C
ENST00000676810.1:c.363+1153G>C ENSP00000503161.1:n.363+1153G>C
ENST00000676996.1:n.573+1153G>C
ENST00000677212.1:n.600+1153G>C
ENST00000678522.1:n.600+1153G>C
ENST00000678566.1:c.366+1153G>C ENSP00000502931.1:n.366+1153G>C
ENST00000678668.1:c.-511+1153G>C ENSP00000504418.1:n.-511+1153G>C
ENST00000678740.1:n.597+1153G>C
ENST00000679104.1:c.*113+1153G>C ENSP00000504157.1:n.*113+1153G>C
ENST00000360534.7:c.366+1153G>C ENSP00000353731.3:n.366+1153G>C
ENST00000413651.3:c.*113+1153G>C ENSP00000410264.1:n.*113+1153G>C
ENST00000416189.5:c.373+1153G>C
ENST00000434918.6:c.363+1153G>C ENSP00000402259.2:n.363+1153G>C
ENST00000461836.5:n.550+1153G>C
ENST00000490286.5:n.360+1153G>C
ENST00000497461.5:n.574+1153G>C
NM_001935.3:c.366+1153G>C NP_001926.2:n.366+1153G>C
XM_005246371.2:c.363+1153G>C XP_005246428.1:n.363+1153G>C
XM_005246371.3:c.363+1153G>C XP_005246428.1:n.363+1153G>C
NM_001935.4:c.366+1153G>C MANE Select NP_001926.2:n.366+1153G>C
NM_001379604.1:c.363+1153G>C NP_001366533.1:n.363+1153G>C
NM_001379605.1:c.360+1153G>C NP_001366534.1:n.360+1153G>C
NM_001379606.1:c.366+1153G>C NP_001366535.1:n.366+1153G>C
NR_166822.1:n.597+1153G>C
NR_166823.1:n.840+1153G>C
NR_166824.1:n.600+1153G>C
NR_166825.1:n.600+1153G>C