Canonical Allele Identifier: CA2838198280

Gene: EVI5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92703758C>A , CM000663.2:g.92703758C>A	GRCh38
NC_000001.10:g.93169315C>A , CM000663.1:g.93169315C>A	GRCh37
NC_000001.9:g.92941903C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540033.3:c.472-139G>T	ENSP00000440826.2:n.472-139G>T
ENST00000706843.1:c.463-139G>T	ENSP00000516584.1:n.463-139G>T
ENST00000706845.1:c.*173-139G>T	ENSP00000516587.1:n.*173-139G>T
ENST00000706846.1:c.340-139G>T	ENSP00000516588.1:n.340-139G>T
ENST00000706847.1:c.340-139G>T	ENSP00000516589.1:n.340-139G>T
ENST00000706867.1:c.420+83G>T	ENSP00000516594.1:n.420+83G>T
ENST00000706868.1:c.340-139G>T	ENSP00000516595.1:n.340-139G>T
ENST00000706869.1:n.309+70230G>T
ENST00000706870.1:n.377-139G>T
ENST00000706883.1:c.-873-139G>T	ENSP00000516600.1:n.-873-139G>T
ENST00000706884.1:n.665-139G>T
ENST00000706885.1:c.205-139G>T	ENSP00000516601.1:n.205-139G>T
ENST00000684568.2:c.340-139G>T MANE Select	ENSP00000506999.1:n.340-139G>T
ENST00000370331.5:c.472-139G>T	ENSP00000359356.1:n.472-139G>T
ENST00000540033.2:c.472-139G>T	ENSP00000440826.2:n.472-139G>T
NM_001308248.1:c.472-139G>T	NP_001295177.1:n.472-139G>T
NM_005665.4:c.472-139G>T	NP_005656.4:n.472-139G>T
NM_005665.5:c.472-139G>T	NP_005656.4:n.472-139G>T
XM_011542099.1:c.543+83G>T	XP_011540401.1:n.543+83G>T
XM_011542100.1:c.543+83G>T	XP_011540402.1:n.543+83G>T
XM_011542101.1:c.420+83G>T	XP_011540403.1:n.420+83G>T
XM_011542102.1:c.543+83G>T	XP_011540404.1:n.543+83G>T
XM_011542103.1:c.543+83G>T	XP_011540405.1:n.543+83G>T
XM_011542104.1:c.543+83G>T	XP_011540406.1:n.543+83G>T
XM_011542105.1:c.543+83G>T	XP_011540407.1:n.543+83G>T
XM_011542107.1:c.472-139G>T	XP_011540409.1:n.472-139G>T
XM_011542108.1:c.543+83G>T	XP_011540410.1:n.543+83G>T
XM_011542109.1:c.543+83G>T	XP_011540411.1:n.543+83G>T
XM_011542110.1:c.543+83G>T	XP_011540412.1:n.543+83G>T
XM_011542111.1:c.543+83G>T	XP_011540413.1:n.543+83G>T
NM_001350197.1:c.340-139G>T	NP_001337126.1:n.340-139G>T
NM_001350198.1:c.340-139G>T	NP_001337127.1:n.340-139G>T
XM_017002269.1:c.552+83G>T	XP_016857758.1:n.552+83G>T
XM_017002270.2:c.543+83G>T	XP_016857759.1:n.543+83G>T
XM_017002271.2:c.472-139G>T	XP_016857760.1:n.472-139G>T
XM_017002272.1:c.552+83G>T	XP_016857761.1:n.552+83G>T
XM_017002273.2:c.420+83G>T	XP_016857762.1:n.420+83G>T
XM_017002274.1:c.420+83G>T	XP_016857763.1:n.420+83G>T
XM_017002275.1:c.420+83G>T	XP_016857764.1:n.420+83G>T
XM_017002276.2:c.340-139G>T	XP_016857765.1:n.340-139G>T
XM_017002277.1:c.472-139G>T	XP_016857766.1:n.472-139G>T
XM_017002278.1:c.552+83G>T	XP_016857767.1:n.552+83G>T
XM_017002279.1:c.285+83G>T	XP_016857768.1:n.285+83G>T
XM_017002281.2:c.463-139G>T	XP_016857770.1:n.463-139G>T
XM_017002282.1:c.552+83G>T	XP_016857771.1:n.552+83G>T
XM_017002283.1:c.472-139G>T	XP_016857772.1:n.472-139G>T
XM_017002284.2:c.340-139G>T	XP_016857773.1:n.340-139G>T
XM_017002286.2:c.-72-139G>T	XP_016857775.1:n.-72-139G>T
XM_017002287.2:c.-73+83G>T	XP_016857776.1:n.-73+83G>T
XM_017002288.1:c.-94G>T	XP_016857777.1:n.-94G>T
XM_024449686.1:c.472-139G>T	XP_024305454.1:n.472-139G>T
XM_024449689.1:c.552+83G>T	XP_024305457.1:n.552+83G>T
XM_024449690.1:c.205-139G>T	XP_024305458.1:n.205-139G>T
XR_001737401.1:n.560+83G>T
NM_001308248.2:c.472-139G>T	NP_001295177.1:n.472-139G>T
NM_001350197.2:c.340-139G>T MANE Select	NP_001337126.1:n.340-139G>T
NM_001350198.2:c.340-139G>T	NP_001337127.1:n.340-139G>T
NM_001377210.1:c.463-139G>T	NP_001364139.1:n.463-139G>T
NM_001377211.1:c.340-139G>T	NP_001364140.1:n.340-139G>T
NM_001377212.1:c.340-139G>T	NP_001364141.1:n.340-139G>T
NM_001377213.1:c.420+83G>T	NP_001364142.1:n.420+83G>T
NM_005665.6:c.472-139G>T	NP_005656.4:n.472-139G>T