Canonical Allele Identifier: CA418958663
Gene: EVI5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.93073168T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92607611T>A , CM000663.2:g.92607611T>A GRCh38
NC_000001.10:g.93073168T>A , CM000663.1:g.93073168T>A GRCh37
NC_000001.9:g.92845756T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000540033.3:c.1929A>T ENSP00000440826.2:p.Ala643=
ENST00000706843.1:c.1920A>T ENSP00000516584.1:p.Ala640=
ENST00000706845.1:c.*1777A>T ENSP00000516587.1:n.*1777A>T
ENST00000706846.1:c.1944A>T ENSP00000516588.1:p.Ala648=
ENST00000706867.1:c.2025A>T ENSP00000516594.1:p.Ala675=
ENST00000706868.1:c.1944A>T ENSP00000516595.1:p.Ala648=
ENST00000706869.1:n.310-3812A>T
ENST00000706883.1:c.732A>T ENSP00000516600.1:p.Ala244=
ENST00000706885.1:c.1809A>T ENSP00000516601.1:p.Ala603=
ENST00000684568.2:c.1944A>T MANE Select ENSP00000506999.1:p.Ala648=
ENST00000370331.5:c.1896A>T ENSP00000359356.1:p.Ala632=
ENST00000491940.5:n.749A>T
ENST00000492513.5:n.417A>T
ENST00000540033.2:c.1929A>T ENSP00000440826.2:p.Ala643=
NM_001308248.1:c.1929A>T NP_001295177.1:p.Ala643=
NM_005665.4:c.1896A>T NP_005656.4:p.Ala632=
NM_005665.5:c.1896A>T NP_005656.4:p.Ala632=
XM_011542099.1:c.2148A>T XP_011540401.1:p.Ala716=
XM_011542100.1:c.2148A>T XP_011540402.1:p.Ala716=
XM_011542101.1:c.2025A>T XP_011540403.1:p.Ala675=
XM_011542102.1:c.2001A>T XP_011540404.1:p.Ala667=
XM_011542103.1:c.2032-2209A>T XP_011540405.1:n.2032-2209A>T
XM_011542104.1:c.1989A>T XP_011540406.1:p.Ala663=
XM_011542105.1:c.1968A>T XP_011540407.1:p.Ala656=
XM_011542107.1:c.1896A>T XP_011540409.1:p.Ala632=
XM_011542108.1:c.2148A>T XP_011540410.1:p.Ala716=
XM_011542109.1:c.2148A>T XP_011540411.1:p.Ala716=
NM_001350197.1:c.1944A>T NP_001337126.1:p.Ala648=
NM_001350198.1:c.1944A>T NP_001337127.1:p.Ala648=
XM_017002269.1:c.2157A>T XP_016857758.1:p.Ala719=
XM_017002270.2:c.2148A>T XP_016857759.1:p.Ala716=
XM_017002271.2:c.2076A>T XP_016857760.1:p.Ala692=
XM_017002272.1:c.2157A>T XP_016857761.1:p.Ala719=
XM_017002273.2:c.2025A>T XP_016857762.1:p.Ala675=
XM_017002274.1:c.2025A>T XP_016857763.1:p.Ala675=
XM_017002275.1:c.2025A>T XP_016857764.1:p.Ala675=
XM_017002276.2:c.1944A>T XP_016857765.1:p.Ala648=
XM_017002277.1:c.1929A>T XP_016857766.1:p.Ala643=
XM_017002278.1:c.2010A>T XP_016857767.1:p.Ala670=
XM_017002279.1:c.1890A>T XP_016857768.1:p.Ala630=
XM_017002281.2:c.1920A>T XP_016857770.1:p.Ala640=
XM_017002282.1:c.2157A>T XP_016857771.1:p.Ala719=
XM_017002283.1:c.2076A>T XP_016857772.1:p.Ala692=
XM_017002284.2:c.1797A>T XP_016857773.1:p.Ala599=
XM_017002286.2:c.1533A>T XP_016857775.1:p.Ala511=
XM_017002287.2:c.1533A>T XP_016857776.1:p.Ala511=
XM_017002288.1:c.1533A>T XP_016857777.1:p.Ala511=
XM_024449686.1:c.2076A>T XP_024305454.1:p.Ala692=
XM_024449689.1:c.1977A>T XP_024305457.1:p.Ala659=
XM_024449690.1:c.1809A>T XP_024305458.1:p.Ala603=
NM_001308248.2:c.1929A>T NP_001295177.1:p.Ala643=
NM_001350197.2:c.1944A>T MANE Select NP_001337126.1:p.Ala648=
NM_001350198.2:c.1944A>T NP_001337127.1:p.Ala648=
NM_001377210.1:c.1920A>T NP_001364139.1:p.Ala640=
NM_001377211.1:c.1902A>T NP_001364140.1:p.Ala634=
NM_001377212.1:c.1797A>T NP_001364141.1:p.Ala599=
NM_001377213.1:c.2025A>T NP_001364142.1:p.Ala675=
NM_005665.6:c.1896A>T NP_005656.4:p.Ala632=