Canonical Allele Identifier: CA352882662
Gene: MST1 HGNC NCBI

Linked Data

dbSNP Id: rs3197999

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49684099G>T , CM000665.2:g.49684099G>T GRCh38
NC_000003.11:g.49721532G>T , CM000665.1:g.49721532G>T GRCh37
NC_000003.10:g.49696536G>T NCBI36
NG_011438.1:g.15098G>T
NG_016454.1:g.9665C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000449682.3:c.2107C>A MANE Select ENSP00000414287.2:p.Arg703Ser
ENST00000448220.5:c.515C>A
ENST00000449682.2:c.2107C>A ENSP00000414287.2:p.Arg703Ser
ENST00000479115.5:n.2162C>A
ENST00000488350.6:n.4029C>A
ENST00000492329.5:n.1883C>A
ENST00000493836.5:n.873C>A
NM_020998.3:c.2107C>A NP_066278.3:p.Arg703Ser
XM_006713166.1:c.1972C>A XP_006713229.1:p.Arg658Ser
XM_011533730.1:c.2242C>A XP_011532032.1:p.Arg748Ser
XM_011533731.1:c.2149C>A XP_011532033.1:p.Arg717Ser
XM_011533732.1:c.2143C>A XP_011532034.1:p.Arg715Ser
XM_011533733.1:c.*27C>A XP_011532035.1:n.*27C>A
XR_427270.2:n.3039C>A
XR_427271.1:n.2990C>A
XR_427273.1:n.2895C>A
XR_427274.2:n.2940C>A
XR_940425.1:n.3035C>A
XR_940426.1:n.3075C>A
XR_940427.1:n.2940C>A
NR_146060.1:n.2060C>A
XM_006713166.2:c.1972C>A XP_006713229.1:p.Arg658Ser
XM_011533732.2:c.2143C>A XP_011532034.1:p.Arg715Ser
XM_017006460.2:c.2086C>A XP_016861949.1:p.Arg696Ser
XM_017006461.2:c.2050C>A XP_016861950.1:p.Arg684Ser
XM_017006462.2:c.*27C>A XP_016861951.1:n.*27C>A
XM_017006463.2:c.*27C>A XP_016861952.1:n.*27C>A
XM_017006464.2:c.*27C>A XP_016861953.1:n.*27C>A
XR_001740149.2:n.2207C>A
XR_001740150.2:n.2204C>A
XR_001740151.2:n.2247C>A
XR_001740152.2:n.2162C>A
XR_001740153.2:n.2208C>A
XR_002959536.1:n.2162C>A
XR_427273.2:n.2166C>A
XR_940427.2:n.2211C>A
NM_001393581.1:c.2143C>A NP_001380510.1:p.Arg715Ser
NM_001393582.1:c.2050C>A NP_001380511.1:p.Arg684Ser
NM_001393583.1:c.2017C>A NP_001380512.1:p.Arg673Ser
NM_001393584.1:c.1972C>A NP_001380513.1:p.Arg658Ser
NM_001393585.1:c.1807C>A NP_001380514.1:p.Arg603Ser
NM_020998.4:c.2107C>A MANE Select NP_066278.3:p.Arg703Ser
NR_146060.2:n.2771C>A