Canonical Allele Identifier: CA1363603367
Gene: MST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49684010A= , CM000665.2:g.49684010A= GRCh38
NC_000003.11:g.49721443A= , CM000665.1:g.49721443A= GRCh37
NC_000003.10:g.49696447A= NCBI36
NG_011438.1:g.15009A=
NG_016454.1:g.9754T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000449682.3:c.*18T= MANE Select ENSP00000414287.2:n.*18T=
ENST00000448220.5:c.604T=
ENST00000449682.2:c.*18T= ENSP00000414287.2:n.*18T=
ENST00000479115.5:n.2251T=
ENST00000488350.6:n.4118T=
ENST00000492329.5:n.1972T=
NM_020998.3:c.*18T= NP_066278.3:n.*18T=
XM_006713166.1:c.*18T= XP_006713229.1:n.*18T=
XM_011533730.1:c.*18T= XP_011532032.1:n.*18T=
XM_011533731.1:c.*18T= XP_011532033.1:n.*18T=
XM_011533732.1:c.*18T= XP_011532034.1:n.*18T=
XM_011533733.1:c.*116T= XP_011532035.1:n.*116T=
XR_427270.2:n.3128T=
XR_427271.1:n.3079T=
XR_427273.1:n.2984T=
XR_427274.2:n.3029T=
XR_940425.1:n.3124T=
XR_940426.1:n.3164T=
XR_940427.1:n.3029T=
NR_146060.1:n.2149T=
XM_006713166.2:c.*18T= XP_006713229.1:n.*18T=
XM_011533732.2:c.*18T= XP_011532034.1:n.*18T=
XM_017006460.2:c.*18T= XP_016861949.1:n.*18T=
XM_017006461.2:c.*18T= XP_016861950.1:n.*18T=
XM_017006462.2:c.*116T= XP_016861951.1:n.*116T=
XM_017006463.2:c.*116T= XP_016861952.1:n.*116T=
XM_017006464.2:c.*116T= XP_016861953.1:n.*116T=
XR_001740149.2:n.2296T=
XR_001740150.2:n.2293T=
XR_001740151.2:n.2336T=
XR_001740152.2:n.2251T=
XR_001740153.2:n.2297T=
XR_002959536.1:n.2251T=
XR_427273.2:n.2255T=
XR_940427.2:n.2300T=
NM_001393581.1:c.*18T= NP_001380510.1:n.*18T=
NM_001393582.1:c.*18T= NP_001380511.1:n.*18T=
NM_001393583.1:c.*18T= NP_001380512.1:n.*18T=
NM_001393584.1:c.*18T= NP_001380513.1:n.*18T=
NM_001393585.1:c.*18T= NP_001380514.1:n.*18T=
NM_020998.4:c.*18T= MANE Select NP_066278.3:n.*18T=
NR_146060.2:n.2860T=