Canonical Allele Identifier: CA1180836776

Gene: EVI5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92607645T= , CM000663.2:g.92607645T=	GRCh38
NC_000001.10:g.93073202T= , CM000663.1:g.93073202T=	GRCh37
NC_000001.9:g.92845790T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540033.3:c.1895A=	ENSP00000440826.2:p.Gln632=
ENST00000706843.1:c.1886A=	ENSP00000516584.1:p.Gln629=
ENST00000706845.1:c.*1743A=	ENSP00000516587.1:n.*1743A=
ENST00000706846.1:c.1910A=	ENSP00000516588.1:p.Gln637=
ENST00000706867.1:c.1991A=	ENSP00000516594.1:p.Gln664=
ENST00000706868.1:c.1910A=	ENSP00000516595.1:p.Gln637=
ENST00000706869.1:n.310-3846A=
ENST00000706883.1:c.698A=	ENSP00000516600.1:p.Gln233=
ENST00000706885.1:c.1775A=	ENSP00000516601.1:p.Gln592=
ENST00000684568.2:c.1910A= MANE Select	ENSP00000506999.1:p.Gln637=
ENST00000370331.5:c.1862A=	ENSP00000359356.1:p.Gln621=
ENST00000468580.5:n.625A=
ENST00000491940.5:n.715A=
ENST00000492513.5:n.383A=
ENST00000540033.2:c.1895A=	ENSP00000440826.2:p.Gln632=
NM_001308248.1:c.1895A=	NP_001295177.1:p.Gln632=
NM_005665.4:c.1862A=	NP_005656.4:p.Gln621=
NM_005665.5:c.1862A=	NP_005656.4:p.Gln621=
XM_011542099.1:c.2114A=	XP_011540401.1:p.Gln705=
XM_011542100.1:c.2114A=	XP_011540402.1:p.Gln705=
XM_011542101.1:c.1991A=	XP_011540403.1:p.Gln664=
XM_011542102.1:c.1967A=	XP_011540404.1:p.Gln656=
XM_011542103.1:c.2032-2243A=	XP_011540405.1:n.2032-2243A=
XM_011542104.1:c.1955A=	XP_011540406.1:p.Gln652=
XM_011542105.1:c.1934A=	XP_011540407.1:p.Gln645=
XM_011542107.1:c.1862A=	XP_011540409.1:p.Gln621=
XM_011542108.1:c.2114A=	XP_011540410.1:p.Gln705=
XM_011542109.1:c.2114A=	XP_011540411.1:p.Gln705=
NM_001350197.1:c.1910A=	NP_001337126.1:p.Gln637=
NM_001350198.1:c.1910A=	NP_001337127.1:p.Gln637=
XM_017002269.1:c.2123A=	XP_016857758.1:p.Gln708=
XM_017002270.2:c.2114A=	XP_016857759.1:p.Gln705=
XM_017002271.2:c.2042A=	XP_016857760.1:p.Gln681=
XM_017002272.1:c.2123A=	XP_016857761.1:p.Gln708=
XM_017002273.2:c.1991A=	XP_016857762.1:p.Gln664=
XM_017002274.1:c.1991A=	XP_016857763.1:p.Gln664=
XM_017002275.1:c.1991A=	XP_016857764.1:p.Gln664=
XM_017002276.2:c.1910A=	XP_016857765.1:p.Gln637=
XM_017002277.1:c.1895A=	XP_016857766.1:p.Gln632=
XM_017002278.1:c.1976A=	XP_016857767.1:p.Gln659=
XM_017002279.1:c.1856A=	XP_016857768.1:p.Gln619=
XM_017002281.2:c.1886A=	XP_016857770.1:p.Gln629=
XM_017002282.1:c.2123A=	XP_016857771.1:p.Gln708=
XM_017002283.1:c.2042A=	XP_016857772.1:p.Gln681=
XM_017002284.2:c.1763A=	XP_016857773.1:p.Gln588=
XM_017002286.2:c.1499A=	XP_016857775.1:p.Gln500=
XM_017002287.2:c.1499A=	XP_016857776.1:p.Gln500=
XM_017002288.1:c.1499A=	XP_016857777.1:p.Gln500=
XM_024449686.1:c.2042A=	XP_024305454.1:p.Gln681=
XM_024449689.1:c.1943A=	XP_024305457.1:p.Gln648=
XM_024449690.1:c.1775A=	XP_024305458.1:p.Gln592=
NM_001308248.2:c.1895A=	NP_001295177.1:p.Gln632=
NM_001350197.2:c.1910A= MANE Select	NP_001337126.1:p.Gln637=
NM_001350198.2:c.1910A=	NP_001337127.1:p.Gln637=
NM_001377210.1:c.1886A=	NP_001364139.1:p.Gln629=
NM_001377211.1:c.1868A=	NP_001364140.1:p.Gln623=
NM_001377212.1:c.1763A=	NP_001364141.1:p.Gln588=
NM_001377213.1:c.1991A=	NP_001364142.1:p.Gln664=
NM_005665.6:c.1862A=	NP_005656.4:p.Gln621=