Canonical Allele Identifier: CA5057862
Gene: MELK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.36671002C>T , CM000671.2:g.36671002C>T GRCh38
NC_000009.11:g.36670999C>T , CM000671.1:g.36670999C>T GRCh37
NC_000009.10:g.36660999C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014791.4:c.1510C>T MANE Select NP_055606.1:p.Arg504Cys
ENST00000298048.7:c.1510C>T MANE Select ENSP00000298048.2:p.Arg504Cys
NM_001256685.1:c.1387C>T NP_001243614.1:p.Arg463Cys
NM_001256685.2:c.1387C>T NP_001243614.1:p.Arg463Cys
NM_001256687.1:c.1366C>T NP_001243616.1:p.Arg456Cys
NM_001256687.2:c.1366C>T NP_001243616.1:p.Arg456Cys
NM_001256688.1:c.1297C>T NP_001243617.1:p.Arg433Cys
NM_001256688.2:c.1297C>T NP_001243617.1:p.Arg433Cys
NM_001256689.1:c.1414C>T NP_001243618.1:p.Arg472Cys
NM_001256689.2:c.1414C>T NP_001243618.1:p.Arg472Cys
NM_001256690.1:c.1297C>T NP_001243619.1:p.Arg433Cys
NM_001256690.2:c.1297C>T NP_001243619.1:p.Arg433Cys
NM_001256691.1:c.1270C>T NP_001243620.1:p.Arg424Cys
NM_001256691.2:c.1270C>T NP_001243620.1:p.Arg424Cys
NM_001256692.1:c.1117C>T NP_001243621.1:p.Arg373Cys
NM_001256692.2:c.1117C>T NP_001243621.1:p.Arg373Cys
NM_001256693.1:c.928C>T NP_001243622.1:p.Arg310Cys
NM_001256693.2:c.928C>T NP_001243622.1:p.Arg310Cys
NM_014791.3:c.1510C>T NP_055606.1:p.Arg504Cys
NR_046337.1:n.1731C>T
NR_046337.2:n.1698C>T
ENST00000298048.6:c.1510C>T ENSP00000298048.2:p.Arg504Cys
ENST00000536329.5:c.1297C>T ENSP00000443550.1:p.Arg433Cys
ENST00000536860.5:c.1366C>T ENSP00000439792.1:p.Arg456Cys
ENST00000536987.5:c.1117C>T ENSP00000439184.1:p.Arg373Cys
ENST00000541717.4:c.1387C>T ENSP00000437804.1:p.Arg463Cys
ENST00000543751.5:c.1414C>T ENSP00000441596.1:p.Arg472Cys
ENST00000545008.5:c.1297C>T ENSP00000445452.1:p.Arg433Cys
ENST00000626154.2:c.*867C>T ENSP00000486558.1:n.*867C>T
ENST00000627766.2:c.*881C>T ENSP00000486459.1:n.*881C>T
XM_011518076.1:c.1510C>T XP_011516378.1:p.Arg504Cys
XM_011518076.2:c.1510C>T XP_011516378.1:p.Arg504Cys
XM_011518077.1:c.1510C>T XP_011516379.1:p.Arg504Cys
XM_011518078.1:c.1510C>T XP_011516380.1:p.Arg504Cys
XM_011518078.2:c.1510C>T XP_011516380.1:p.Arg504Cys
XM_011518079.1:c.1510C>T XP_011516381.1:p.Arg504Cys
XM_011518080.1:c.1423C>T XP_011516382.1:p.Arg475Cys
XM_011518081.1:c.1414C>T XP_011516383.1:p.Arg472Cys
XM_011518081.2:c.1414C>T XP_011516383.1:p.Arg472Cys
XM_011518082.1:c.1414C>T XP_011516384.1:p.Arg472Cys
XM_011518082.2:c.1414C>T XP_011516384.1:p.Arg472Cys
XM_011518083.1:c.1414C>T XP_011516385.1:p.Arg472Cys
XM_011518083.2:c.1414C>T XP_011516385.1:p.Arg472Cys
XM_011518084.1:c.1414C>T XP_011516386.1:p.Arg472Cys
XM_011518084.2:c.1414C>T XP_011516386.1:p.Arg472Cys
XM_011518085.1:c.1261C>T XP_011516387.1:p.Arg421Cys