Canonical Allele Identifier: CA418958734

Gene: EVI5

Linked Data

• MyVariant Identifiers: chr1:g.93073183A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92607626A>C , CM000663.2:g.92607626A>C	GRCh38
NC_000001.10:g.93073183A>C , CM000663.1:g.93073183A>C	GRCh37
NC_000001.9:g.92845771A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540033.3:c.1914T>G	ENSP00000440826.2:p.Thr638=
ENST00000706843.1:c.1905T>G	ENSP00000516584.1:p.Thr635=
ENST00000706845.1:c.*1762T>G	ENSP00000516587.1:n.*1762T>G
ENST00000706846.1:c.1929T>G	ENSP00000516588.1:p.Thr643=
ENST00000706867.1:c.2010T>G	ENSP00000516594.1:p.Thr670=
ENST00000706868.1:c.1929T>G	ENSP00000516595.1:p.Thr643=
ENST00000706869.1:n.310-3827T>G
ENST00000706883.1:c.717T>G	ENSP00000516600.1:p.Thr239=
ENST00000706885.1:c.1794T>G	ENSP00000516601.1:p.Thr598=
ENST00000684568.2:c.1929T>G MANE Select	ENSP00000506999.1:p.Thr643=
ENST00000370331.5:c.1881T>G	ENSP00000359356.1:p.Thr627=
ENST00000468580.5:n.644T>G
ENST00000491940.5:n.734T>G
ENST00000492513.5:n.402T>G
ENST00000540033.2:c.1914T>G	ENSP00000440826.2:p.Thr638=
NM_001308248.1:c.1914T>G	NP_001295177.1:p.Thr638=
NM_005665.4:c.1881T>G	NP_005656.4:p.Thr627=
NM_005665.5:c.1881T>G	NP_005656.4:p.Thr627=
XM_011542099.1:c.2133T>G	XP_011540401.1:p.Thr711=
XM_011542100.1:c.2133T>G	XP_011540402.1:p.Thr711=
XM_011542101.1:c.2010T>G	XP_011540403.1:p.Thr670=
XM_011542102.1:c.1986T>G	XP_011540404.1:p.Thr662=
XM_011542103.1:c.2032-2224T>G	XP_011540405.1:n.2032-2224T>G
XM_011542104.1:c.1974T>G	XP_011540406.1:p.Thr658=
XM_011542105.1:c.1953T>G	XP_011540407.1:p.Thr651=
XM_011542107.1:c.1881T>G	XP_011540409.1:p.Thr627=
XM_011542108.1:c.2133T>G	XP_011540410.1:p.Thr711=
XM_011542109.1:c.2133T>G	XP_011540411.1:p.Thr711=
NM_001350197.1:c.1929T>G	NP_001337126.1:p.Thr643=
NM_001350198.1:c.1929T>G	NP_001337127.1:p.Thr643=
XM_017002269.1:c.2142T>G	XP_016857758.1:p.Thr714=
XM_017002270.2:c.2133T>G	XP_016857759.1:p.Thr711=
XM_017002271.2:c.2061T>G	XP_016857760.1:p.Thr687=
XM_017002272.1:c.2142T>G	XP_016857761.1:p.Thr714=
XM_017002273.2:c.2010T>G	XP_016857762.1:p.Thr670=
XM_017002274.1:c.2010T>G	XP_016857763.1:p.Thr670=
XM_017002275.1:c.2010T>G	XP_016857764.1:p.Thr670=
XM_017002276.2:c.1929T>G	XP_016857765.1:p.Thr643=
XM_017002277.1:c.1914T>G	XP_016857766.1:p.Thr638=
XM_017002278.1:c.1995T>G	XP_016857767.1:p.Thr665=
XM_017002279.1:c.1875T>G	XP_016857768.1:p.Thr625=
XM_017002281.2:c.1905T>G	XP_016857770.1:p.Thr635=
XM_017002282.1:c.2142T>G	XP_016857771.1:p.Thr714=
XM_017002283.1:c.2061T>G	XP_016857772.1:p.Thr687=
XM_017002284.2:c.1782T>G	XP_016857773.1:p.Thr594=
XM_017002286.2:c.1518T>G	XP_016857775.1:p.Thr506=
XM_017002287.2:c.1518T>G	XP_016857776.1:p.Thr506=
XM_017002288.1:c.1518T>G	XP_016857777.1:p.Thr506=
XM_024449686.1:c.2061T>G	XP_024305454.1:p.Thr687=
XM_024449689.1:c.1962T>G	XP_024305457.1:p.Thr654=
XM_024449690.1:c.1794T>G	XP_024305458.1:p.Thr598=
NM_001308248.2:c.1914T>G	NP_001295177.1:p.Thr638=
NM_001350197.2:c.1929T>G MANE Select	NP_001337126.1:p.Thr643=
NM_001350198.2:c.1929T>G	NP_001337127.1:p.Thr643=
NM_001377210.1:c.1905T>G	NP_001364139.1:p.Thr635=
NM_001377211.1:c.1887T>G	NP_001364140.1:p.Thr629=
NM_001377212.1:c.1782T>G	NP_001364141.1:p.Thr594=
NM_001377213.1:c.2010T>G	NP_001364142.1:p.Thr670=
NM_005665.6:c.1881T>G	NP_005656.4:p.Thr627=