Canonical Allele Identifier: CA15153107

Gene: DPP4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162053713G>C , CM000664.2:g.162053713G>C	GRCh38
NC_000002.11:g.162910223G>C , CM000664.1:g.162910223G>C	GRCh37
NC_000002.10:g.162618469G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360534.8:c.95-6212C>G MANE Select	ENSP00000353731.3:n.95-6212C>G
ENST00000416189.6:c.95-6212C>G	ENSP00000401359.2:n.95-6212C>G
ENST00000461836.6:n.576-6212C>G
ENST00000494507.2:c.95-6212C>G	ENSP00000503735.1:n.95-6212C>G
ENST00000676479.1:c.231-6212C>G	ENSP00000504273.1:n.231-6212C>G
ENST00000676624.1:c.95-6215C>G	ENSP00000503481.1:n.95-6215C>G
ENST00000676768.1:c.95-6212C>G	ENSP00000503008.1:n.95-6212C>G
ENST00000676810.1:c.95-6215C>G	ENSP00000503161.1:n.95-6215C>G
ENST00000676996.1:n.89-6212C>G
ENST00000677212.1:n.116-6212C>G
ENST00000678522.1:n.116-6212C>G
ENST00000678566.1:c.95-6212C>G	ENSP00000502931.1:n.95-6212C>G
ENST00000678668.1:c.-782-6212C>G	ENSP00000504418.1:n.-782-6212C>G
ENST00000678740.1:n.116-6215C>G
ENST00000679104.1:c.95-6212C>G	ENSP00000504157.1:n.95-6212C>G
ENST00000360534.7:c.95-6212C>G	ENSP00000353731.3:n.95-6212C>G
ENST00000413651.3:c.95-6212C>G	ENSP00000410264.1:n.95-6212C>G
ENST00000434918.6:c.95-6215C>G	ENSP00000402259.2:n.95-6215C>G
ENST00000461836.5:n.66-6212C>G
ENST00000490286.5:n.89-6212C>G
ENST00000497461.5:n.199-6212C>G
ENST00000628861.1:c.95-6212C>G	ENSP00000486421.1:n.95-6212C>G
NM_001935.3:c.95-6212C>G	NP_001926.2:n.95-6212C>G
XM_005246371.2:c.95-6215C>G	XP_005246428.1:n.95-6215C>G
XM_005246371.3:c.95-6215C>G	XP_005246428.1:n.95-6215C>G
NM_001935.4:c.95-6212C>G MANE Select	NP_001926.2:n.95-6212C>G
NM_001379604.1:c.95-6215C>G	NP_001366533.1:n.95-6215C>G
NM_001379605.1:c.92-6215C>G	NP_001366534.1:n.92-6215C>G
NM_001379606.1:c.95-6212C>G	NP_001366535.1:n.95-6212C>G
NR_166822.1:n.329-6215C>G
NR_166823.1:n.465-6212C>G
NR_166824.1:n.329-6212C>G
NR_166825.1:n.329-6212C>G