Canonical Allele Identifier: CA341151930

Gene: EVI5

Linked Data

• MyVariant Identifiers: chr1:g.93073170C>A (hg19) ; chr1:g.92607613C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92607613C>A , CM000663.2:g.92607613C>A	GRCh38
NC_000001.10:g.93073170C>A , CM000663.1:g.93073170C>A	GRCh37
NC_000001.9:g.92845758C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540033.3:c.1927G>T	ENSP00000440826.2:p.Ala643Ser
ENST00000706843.1:c.1918G>T	ENSP00000516584.1:p.Ala640Ser
ENST00000706845.1:c.*1775G>T	ENSP00000516587.1:n.*1775G>T
ENST00000706846.1:c.1942G>T	ENSP00000516588.1:p.Ala648Ser
ENST00000706867.1:c.2023G>T	ENSP00000516594.1:p.Ala675Ser
ENST00000706868.1:c.1942G>T	ENSP00000516595.1:p.Ala648Ser
ENST00000706869.1:n.310-3814G>T
ENST00000706883.1:c.730G>T	ENSP00000516600.1:p.Ala244Ser
ENST00000706885.1:c.1807G>T	ENSP00000516601.1:p.Ala603Ser
ENST00000684568.2:c.1942G>T MANE Select	ENSP00000506999.1:p.Ala648Ser
ENST00000370331.5:c.1894G>T	ENSP00000359356.1:p.Ala632Ser
ENST00000491940.5:n.747G>T
ENST00000492513.5:n.415G>T
ENST00000540033.2:c.1927G>T	ENSP00000440826.2:p.Ala643Ser
NM_001308248.1:c.1927G>T	NP_001295177.1:p.Ala643Ser
NM_005665.4:c.1894G>T	NP_005656.4:p.Ala632Ser
NM_005665.5:c.1894G>T	NP_005656.4:p.Ala632Ser
XM_011542099.1:c.2146G>T	XP_011540401.1:p.Ala716Ser
XM_011542100.1:c.2146G>T	XP_011540402.1:p.Ala716Ser
XM_011542101.1:c.2023G>T	XP_011540403.1:p.Ala675Ser
XM_011542102.1:c.1999G>T	XP_011540404.1:p.Ala667Ser
XM_011542103.1:c.2032-2211G>T	XP_011540405.1:n.2032-2211G>T
XM_011542104.1:c.1987G>T	XP_011540406.1:p.Ala663Ser
XM_011542105.1:c.1966G>T	XP_011540407.1:p.Ala656Ser
XM_011542107.1:c.1894G>T	XP_011540409.1:p.Ala632Ser
XM_011542108.1:c.2146G>T	XP_011540410.1:p.Ala716Ser
XM_011542109.1:c.2146G>T	XP_011540411.1:p.Ala716Ser
NM_001350197.1:c.1942G>T	NP_001337126.1:p.Ala648Ser
NM_001350198.1:c.1942G>T	NP_001337127.1:p.Ala648Ser
XM_017002269.1:c.2155G>T	XP_016857758.1:p.Ala719Ser
XM_017002270.2:c.2146G>T	XP_016857759.1:p.Ala716Ser
XM_017002271.2:c.2074G>T	XP_016857760.1:p.Ala692Ser
XM_017002272.1:c.2155G>T	XP_016857761.1:p.Ala719Ser
XM_017002273.2:c.2023G>T	XP_016857762.1:p.Ala675Ser
XM_017002274.1:c.2023G>T	XP_016857763.1:p.Ala675Ser
XM_017002275.1:c.2023G>T	XP_016857764.1:p.Ala675Ser
XM_017002276.2:c.1942G>T	XP_016857765.1:p.Ala648Ser
XM_017002277.1:c.1927G>T	XP_016857766.1:p.Ala643Ser
XM_017002278.1:c.2008G>T	XP_016857767.1:p.Ala670Ser
XM_017002279.1:c.1888G>T	XP_016857768.1:p.Ala630Ser
XM_017002281.2:c.1918G>T	XP_016857770.1:p.Ala640Ser
XM_017002282.1:c.2155G>T	XP_016857771.1:p.Ala719Ser
XM_017002283.1:c.2074G>T	XP_016857772.1:p.Ala692Ser
XM_017002284.2:c.1795G>T	XP_016857773.1:p.Ala599Ser
XM_017002286.2:c.1531G>T	XP_016857775.1:p.Ala511Ser
XM_017002287.2:c.1531G>T	XP_016857776.1:p.Ala511Ser
XM_017002288.1:c.1531G>T	XP_016857777.1:p.Ala511Ser
XM_024449686.1:c.2074G>T	XP_024305454.1:p.Ala692Ser
XM_024449689.1:c.1975G>T	XP_024305457.1:p.Ala659Ser
XM_024449690.1:c.1807G>T	XP_024305458.1:p.Ala603Ser
NM_001308248.2:c.1927G>T	NP_001295177.1:p.Ala643Ser
NM_001350197.2:c.1942G>T MANE Select	NP_001337126.1:p.Ala648Ser
NM_001350198.2:c.1942G>T	NP_001337127.1:p.Ala648Ser
NM_001377210.1:c.1918G>T	NP_001364139.1:p.Ala640Ser
NM_001377211.1:c.1900G>T	NP_001364140.1:p.Ala634Ser
NM_001377212.1:c.1795G>T	NP_001364141.1:p.Ala599Ser
NM_001377213.1:c.2023G>T	NP_001364142.1:p.Ala675Ser
NM_005665.6:c.1894G>T	NP_005656.4:p.Ala632Ser