Canonical Allele Identifier: CA341152033

Gene: EVI5

Linked Data

• MyVariant Identifiers: chr1:g.93073195T>G (hg19) ; chr1:g.92607638T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92607638T>G , CM000663.2:g.92607638T>G	GRCh38
NC_000001.10:g.93073195T>G , CM000663.1:g.93073195T>G	GRCh37
NC_000001.9:g.92845783T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540033.3:c.1902A>C	ENSP00000440826.2:p.Lys634Asn
ENST00000706843.1:c.1893A>C	ENSP00000516584.1:p.Lys631Asn
ENST00000706845.1:c.*1750A>C	ENSP00000516587.1:n.*1750A>C
ENST00000706846.1:c.1917A>C	ENSP00000516588.1:p.Lys639Asn
ENST00000706867.1:c.1998A>C	ENSP00000516594.1:p.Lys666Asn
ENST00000706868.1:c.1917A>C	ENSP00000516595.1:p.Lys639Asn
ENST00000706869.1:n.310-3839A>C
ENST00000706883.1:c.705A>C	ENSP00000516600.1:p.Lys235Asn
ENST00000706885.1:c.1782A>C	ENSP00000516601.1:p.Lys594Asn
ENST00000684568.2:c.1917A>C MANE Select	ENSP00000506999.1:p.Lys639Asn
ENST00000370331.5:c.1869A>C	ENSP00000359356.1:p.Lys623Asn
ENST00000468580.5:n.632A>C
ENST00000491940.5:n.722A>C
ENST00000492513.5:n.390A>C
ENST00000540033.2:c.1902A>C	ENSP00000440826.2:p.Lys634Asn
NM_001308248.1:c.1902A>C	NP_001295177.1:p.Lys634Asn
NM_005665.4:c.1869A>C	NP_005656.4:p.Lys623Asn
NM_005665.5:c.1869A>C	NP_005656.4:p.Lys623Asn
XM_011542099.1:c.2121A>C	XP_011540401.1:p.Lys707Asn
XM_011542100.1:c.2121A>C	XP_011540402.1:p.Lys707Asn
XM_011542101.1:c.1998A>C	XP_011540403.1:p.Lys666Asn
XM_011542102.1:c.1974A>C	XP_011540404.1:p.Lys658Asn
XM_011542103.1:c.2032-2236A>C	XP_011540405.1:n.2032-2236A>C
XM_011542104.1:c.1962A>C	XP_011540406.1:p.Lys654Asn
XM_011542105.1:c.1941A>C	XP_011540407.1:p.Lys647Asn
XM_011542107.1:c.1869A>C	XP_011540409.1:p.Lys623Asn
XM_011542108.1:c.2121A>C	XP_011540410.1:p.Lys707Asn
XM_011542109.1:c.2121A>C	XP_011540411.1:p.Lys707Asn
NM_001350197.1:c.1917A>C	NP_001337126.1:p.Lys639Asn
NM_001350198.1:c.1917A>C	NP_001337127.1:p.Lys639Asn
XM_017002269.1:c.2130A>C	XP_016857758.1:p.Lys710Asn
XM_017002270.2:c.2121A>C	XP_016857759.1:p.Lys707Asn
XM_017002271.2:c.2049A>C	XP_016857760.1:p.Lys683Asn
XM_017002272.1:c.2130A>C	XP_016857761.1:p.Lys710Asn
XM_017002273.2:c.1998A>C	XP_016857762.1:p.Lys666Asn
XM_017002274.1:c.1998A>C	XP_016857763.1:p.Lys666Asn
XM_017002275.1:c.1998A>C	XP_016857764.1:p.Lys666Asn
XM_017002276.2:c.1917A>C	XP_016857765.1:p.Lys639Asn
XM_017002277.1:c.1902A>C	XP_016857766.1:p.Lys634Asn
XM_017002278.1:c.1983A>C	XP_016857767.1:p.Lys661Asn
XM_017002279.1:c.1863A>C	XP_016857768.1:p.Lys621Asn
XM_017002281.2:c.1893A>C	XP_016857770.1:p.Lys631Asn
XM_017002282.1:c.2130A>C	XP_016857771.1:p.Lys710Asn
XM_017002283.1:c.2049A>C	XP_016857772.1:p.Lys683Asn
XM_017002284.2:c.1770A>C	XP_016857773.1:p.Lys590Asn
XM_017002286.2:c.1506A>C	XP_016857775.1:p.Lys502Asn
XM_017002287.2:c.1506A>C	XP_016857776.1:p.Lys502Asn
XM_017002288.1:c.1506A>C	XP_016857777.1:p.Lys502Asn
XM_024449686.1:c.2049A>C	XP_024305454.1:p.Lys683Asn
XM_024449689.1:c.1950A>C	XP_024305457.1:p.Lys650Asn
XM_024449690.1:c.1782A>C	XP_024305458.1:p.Lys594Asn
NM_001308248.2:c.1902A>C	NP_001295177.1:p.Lys634Asn
NM_001350197.2:c.1917A>C MANE Select	NP_001337126.1:p.Lys639Asn
NM_001350198.2:c.1917A>C	NP_001337127.1:p.Lys639Asn
NM_001377210.1:c.1893A>C	NP_001364139.1:p.Lys631Asn
NM_001377211.1:c.1875A>C	NP_001364140.1:p.Lys625Asn
NM_001377212.1:c.1770A>C	NP_001364141.1:p.Lys590Asn
NM_001377213.1:c.1998A>C	NP_001364142.1:p.Lys666Asn
NM_005665.6:c.1869A>C	NP_005656.4:p.Lys623Asn