Canonical Allele Identifier: CA1180836657
Gene: EVI5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92607523_92607525delinsCAA , CM000663.2:g.92607523_92607525delinsCAA GRCh38
NC_000001.10:g.93073080_93073082delinsCAA , CM000663.1:g.93073080_93073082delinsCAA GRCh37
NC_000001.9:g.92845668_92845670delinsCAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000540033.3:c.1959+56_1959+58delinsTTG ENSP00000440826.2:n.1959+56_1959+58delinsTTG
ENST00000706843.1:c.1950+56_1950+58delinsTTG ENSP00000516584.1:n.1950+56_1950+58delinsTTG
ENST00000706845.1:c.*1807+56_*1807+58delinsTTG ENSP00000516587.1:n.*1807+56_*1807+58delinsTTG
ENST00000706846.1:c.1974+56_1974+58delinsTTG ENSP00000516588.1:n.1974+56_1974+58delinsTTG
ENST00000706867.1:c.2055+56_2055+58delinsTTG ENSP00000516594.1:n.2055+56_2055+58delinsTTG
ENST00000706868.1:c.1974+56_1974+58delinsTTG ENSP00000516595.1:n.1974+56_1974+58delinsTTG
ENST00000706869.1:n.310-3726_310-3724delinsTTG
ENST00000706883.1:c.762+56_762+58delinsTTG ENSP00000516600.1:n.762+56_762+58delinsTTG
ENST00000706885.1:c.1839+56_1839+58delinsTTG ENSP00000516601.1:n.1839+56_1839+58delinsTTG
ENST00000684568.2:c.1974+56_1974+58delinsTTG MANE Select ENSP00000506999.1:n.1974+56_1974+58delinsTTG
ENST00000370331.5:c.1926+56_1926+58delinsTTG ENSP00000359356.1:n.1926+56_1926+58delinsTTG
ENST00000491940.5:n.779+56_779+58delinsTTG
ENST00000492513.5:n.503_505delinsTTG
ENST00000540033.2:c.1959+56_1959+58delinsTTG ENSP00000440826.2:n.1959+56_1959+58delinsTTG
NM_001308248.1:c.1959+56_1959+58delinsTTG NP_001295177.1:n.1959+56_1959+58delinsTTG
NM_005665.4:c.1926+56_1926+58delinsTTG NP_005656.4:n.1926+56_1926+58delinsTTG
NM_005665.5:c.1926+56_1926+58delinsTTG NP_005656.4:n.1926+56_1926+58delinsTTG
XM_011542099.1:c.2178+56_2178+58delinsTTG XP_011540401.1:n.2178+56_2178+58delinsTTG
XM_011542100.1:c.2178+56_2178+58delinsTTG XP_011540402.1:n.2178+56_2178+58delinsTTG
XM_011542101.1:c.2055+56_2055+58delinsTTG XP_011540403.1:n.2055+56_2055+58delinsTTG
XM_011542102.1:c.2031+56_2031+58delinsTTG XP_011540404.1:n.2031+56_2031+58delinsTTG
XM_011542103.1:c.2032-2123_2032-2121delinsTTG XP_011540405.1:n.2032-2123_2032-2121delinsTTG
XM_011542104.1:c.2019+56_2019+58delinsTTG XP_011540406.1:n.2019+56_2019+58delinsTTG
XM_011542105.1:c.1998+56_1998+58delinsTTG XP_011540407.1:n.1998+56_1998+58delinsTTG
XM_011542107.1:c.1926+56_1926+58delinsTTG XP_011540409.1:n.1926+56_1926+58delinsTTG
XM_011542108.1:c.2178+56_2178+58delinsTTG XP_011540410.1:n.2178+56_2178+58delinsTTG
XM_011542109.1:c.2178+56_2178+58delinsTTG XP_011540411.1:n.2178+56_2178+58delinsTTG
NM_001350197.1:c.1974+56_1974+58delinsTTG NP_001337126.1:n.1974+56_1974+58delinsTTG
NM_001350198.1:c.1974+56_1974+58delinsTTG NP_001337127.1:n.1974+56_1974+58delinsTTG
XM_017002269.1:c.2187+56_2187+58delinsTTG XP_016857758.1:n.2187+56_2187+58delinsTTG
XM_017002270.2:c.2178+56_2178+58delinsTTG XP_016857759.1:n.2178+56_2178+58delinsTTG
XM_017002271.2:c.2106+56_2106+58delinsTTG XP_016857760.1:n.2106+56_2106+58delinsTTG
XM_017002272.1:c.2187+56_2187+58delinsTTG XP_016857761.1:n.2187+56_2187+58delinsTTG
XM_017002273.2:c.2055+56_2055+58delinsTTG XP_016857762.1:n.2055+56_2055+58delinsTTG
XM_017002274.1:c.2055+56_2055+58delinsTTG XP_016857763.1:n.2055+56_2055+58delinsTTG
XM_017002275.1:c.2055+56_2055+58delinsTTG XP_016857764.1:n.2055+56_2055+58delinsTTG
XM_017002276.2:c.1974+56_1974+58delinsTTG XP_016857765.1:n.1974+56_1974+58delinsTTG
XM_017002277.1:c.1959+56_1959+58delinsTTG XP_016857766.1:n.1959+56_1959+58delinsTTG
XM_017002278.1:c.2040+56_2040+58delinsTTG XP_016857767.1:n.2040+56_2040+58delinsTTG
XM_017002279.1:c.1920+56_1920+58delinsTTG XP_016857768.1:n.1920+56_1920+58delinsTTG
XM_017002281.2:c.1950+56_1950+58delinsTTG XP_016857770.1:n.1950+56_1950+58delinsTTG
XM_017002282.1:c.2187+56_2187+58delinsTTG XP_016857771.1:n.2187+56_2187+58delinsTTG
XM_017002283.1:c.2106+56_2106+58delinsTTG XP_016857772.1:n.2106+56_2106+58delinsTTG
XM_017002284.2:c.1827+56_1827+58delinsTTG XP_016857773.1:n.1827+56_1827+58delinsTTG
XM_017002286.2:c.1563+56_1563+58delinsTTG XP_016857775.1:n.1563+56_1563+58delinsTTG
XM_017002287.2:c.1563+56_1563+58delinsTTG XP_016857776.1:n.1563+56_1563+58delinsTTG
XM_017002288.1:c.1563+56_1563+58delinsTTG XP_016857777.1:n.1563+56_1563+58delinsTTG
XM_024449686.1:c.2106+56_2106+58delinsTTG XP_024305454.1:n.2106+56_2106+58delinsTTG
XM_024449689.1:c.2007+56_2007+58delinsTTG XP_024305457.1:n.2007+56_2007+58delinsTTG
XM_024449690.1:c.1839+56_1839+58delinsTTG XP_024305458.1:n.1839+56_1839+58delinsTTG
NM_001308248.2:c.1959+56_1959+58delinsTTG NP_001295177.1:n.1959+56_1959+58delinsTTG
NM_001350197.2:c.1974+56_1974+58delinsTTG MANE Select NP_001337126.1:n.1974+56_1974+58delinsTTG
NM_001350198.2:c.1974+56_1974+58delinsTTG NP_001337127.1:n.1974+56_1974+58delinsTTG
NM_001377210.1:c.1950+56_1950+58delinsTTG NP_001364139.1:n.1950+56_1950+58delinsTTG
NM_001377211.1:c.1932+56_1932+58delinsTTG NP_001364140.1:n.1932+56_1932+58delinsTTG
NM_001377212.1:c.1827+56_1827+58delinsTTG NP_001364141.1:n.1827+56_1827+58delinsTTG
NM_001377213.1:c.2055+56_2055+58delinsTTG NP_001364142.1:n.2055+56_2055+58delinsTTG
NM_005665.6:c.1926+56_1926+58delinsTTG NP_005656.4:n.1926+56_1926+58delinsTTG
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