Canonical Allele Identifier: CA1180836825

Gene: EVI5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92607698T= , CM000663.2:g.92607698T=	GRCh38
NC_000001.10:g.93073255T= , CM000663.1:g.93073255T=	GRCh37
NC_000001.9:g.92845843T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540033.3:c.1842A=	ENSP00000440826.2:p.Arg614=
ENST00000706843.1:c.1833A=	ENSP00000516584.1:p.Arg611=
ENST00000706845.1:c.*1690A=	ENSP00000516587.1:n.*1690A=
ENST00000706846.1:c.1857A=	ENSP00000516588.1:p.Arg619=
ENST00000706867.1:c.1938A=	ENSP00000516594.1:p.Arg646=
ENST00000706868.1:c.1857A=	ENSP00000516595.1:p.Arg619=
ENST00000706869.1:n.310-3899A=
ENST00000706883.1:c.645A=	ENSP00000516600.1:p.Arg215=
ENST00000706885.1:c.1722A=	ENSP00000516601.1:p.Arg574=
ENST00000684568.2:c.1857A= MANE Select	ENSP00000506999.1:p.Arg619=
ENST00000370331.5:c.1809A=	ENSP00000359356.1:p.Arg603=
ENST00000468580.5:n.572A=
ENST00000491940.5:n.662A=
ENST00000492513.5:n.330A=
ENST00000540033.2:c.1842A=	ENSP00000440826.2:p.Arg614=
NM_001308248.1:c.1842A=	NP_001295177.1:p.Arg614=
NM_005665.4:c.1809A=	NP_005656.4:p.Arg603=
NM_005665.5:c.1809A=	NP_005656.4:p.Arg603=
XM_011542099.1:c.2061A=	XP_011540401.1:p.Arg687=
XM_011542100.1:c.2061A=	XP_011540402.1:p.Arg687=
XM_011542101.1:c.1938A=	XP_011540403.1:p.Arg646=
XM_011542102.1:c.1914A=	XP_011540404.1:p.Arg638=
XM_011542103.1:c.2032-2296A=	XP_011540405.1:n.2032-2296A=
XM_011542104.1:c.1902A=	XP_011540406.1:p.Arg634=
XM_011542105.1:c.1881A=	XP_011540407.1:p.Arg627=
XM_011542107.1:c.1809A=	XP_011540409.1:p.Arg603=
XM_011542108.1:c.2061A=	XP_011540410.1:p.Arg687=
XM_011542109.1:c.2061A=	XP_011540411.1:p.Arg687=
NM_001350197.1:c.1857A=	NP_001337126.1:p.Arg619=
NM_001350198.1:c.1857A=	NP_001337127.1:p.Arg619=
XM_017002269.1:c.2070A=	XP_016857758.1:p.Arg690=
XM_017002270.2:c.2061A=	XP_016857759.1:p.Arg687=
XM_017002271.2:c.1989A=	XP_016857760.1:p.Arg663=
XM_017002272.1:c.2070A=	XP_016857761.1:p.Arg690=
XM_017002273.2:c.1938A=	XP_016857762.1:p.Arg646=
XM_017002274.1:c.1938A=	XP_016857763.1:p.Arg646=
XM_017002275.1:c.1938A=	XP_016857764.1:p.Arg646=
XM_017002276.2:c.1857A=	XP_016857765.1:p.Arg619=
XM_017002277.1:c.1842A=	XP_016857766.1:p.Arg614=
XM_017002278.1:c.1923A=	XP_016857767.1:p.Arg641=
XM_017002279.1:c.1803A=	XP_016857768.1:p.Arg601=
XM_017002281.2:c.1833A=	XP_016857770.1:p.Arg611=
XM_017002282.1:c.2070A=	XP_016857771.1:p.Arg690=
XM_017002283.1:c.1989A=	XP_016857772.1:p.Arg663=
XM_017002284.2:c.1710A=	XP_016857773.1:p.Arg570=
XM_017002286.2:c.1446A=	XP_016857775.1:p.Arg482=
XM_017002287.2:c.1446A=	XP_016857776.1:p.Arg482=
XM_017002288.1:c.1446A=	XP_016857777.1:p.Arg482=
XM_024449686.1:c.1989A=	XP_024305454.1:p.Arg663=
XM_024449689.1:c.1890A=	XP_024305457.1:p.Arg630=
XM_024449690.1:c.1722A=	XP_024305458.1:p.Arg574=
NM_001308248.2:c.1842A=	NP_001295177.1:p.Arg614=
NM_001350197.2:c.1857A= MANE Select	NP_001337126.1:p.Arg619=
NM_001350198.2:c.1857A=	NP_001337127.1:p.Arg619=
NM_001377210.1:c.1833A=	NP_001364139.1:p.Arg611=
NM_001377211.1:c.1815A=	NP_001364140.1:p.Arg605=
NM_001377212.1:c.1710A=	NP_001364141.1:p.Arg570=
NM_001377213.1:c.1938A=	NP_001364142.1:p.Arg646=
NM_005665.6:c.1809A=	NP_005656.4:p.Arg603=