Canonical Allele Identifier: CA1363603420
Gene: MST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49684103C= , CM000665.2:g.49684103C= GRCh38
NC_000003.11:g.49721536C= , CM000665.1:g.49721536C= GRCh37
NC_000003.10:g.49696540C= NCBI36
NG_011438.1:g.15102C=
NG_016454.1:g.9661G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000449682.3:c.2103G= MANE Select ENSP00000414287.2:p.Arg701=
ENST00000448220.5:c.511G=
ENST00000449682.2:c.2103G= ENSP00000414287.2:p.Arg701=
ENST00000479115.5:n.2158G=
ENST00000488350.6:n.4025G=
ENST00000492329.5:n.1879G=
ENST00000493836.5:n.869G=
NM_020998.3:c.2103G= NP_066278.3:p.Arg701=
XM_006713166.1:c.1968G= XP_006713229.1:p.Arg656=
XM_011533730.1:c.2238G= XP_011532032.1:p.Arg746=
XM_011533731.1:c.2145G= XP_011532033.1:p.Arg715=
XM_011533732.1:c.2139G= XP_011532034.1:p.Arg713=
XM_011533733.1:c.*23G= XP_011532035.1:n.*23G=
XR_427270.2:n.3035G=
XR_427271.1:n.2986G=
XR_427273.1:n.2891G=
XR_427274.2:n.2936G=
XR_940425.1:n.3031G=
XR_940426.1:n.3071G=
XR_940427.1:n.2936G=
NR_146060.1:n.2056G=
XM_006713166.2:c.1968G= XP_006713229.1:p.Arg656=
XM_011533732.2:c.2139G= XP_011532034.1:p.Arg713=
XM_017006460.2:c.2082G= XP_016861949.1:p.Arg694=
XM_017006461.2:c.2046G= XP_016861950.1:p.Arg682=
XM_017006462.2:c.*23G= XP_016861951.1:n.*23G=
XM_017006463.2:c.*23G= XP_016861952.1:n.*23G=
XM_017006464.2:c.*23G= XP_016861953.1:n.*23G=
XR_001740149.2:n.2203G=
XR_001740150.2:n.2200G=
XR_001740151.2:n.2243G=
XR_001740152.2:n.2158G=
XR_001740153.2:n.2204G=
XR_002959536.1:n.2158G=
XR_427273.2:n.2162G=
XR_940427.2:n.2207G=
NM_001393581.1:c.2139G= NP_001380510.1:p.Arg713=
NM_001393582.1:c.2046G= NP_001380511.1:p.Arg682=
NM_001393583.1:c.2013G= NP_001380512.1:p.Arg671=
NM_001393584.1:c.1968G= NP_001380513.1:p.Arg656=
NM_001393585.1:c.1803G= NP_001380514.1:p.Arg601=
NM_020998.4:c.2103G= MANE Select NP_066278.3:p.Arg701=
NR_146060.2:n.2767G=