Canonical Allele Identifier: CA352882661
Community Standard Title: NM_020998.4(MST1):c.2107C>G (p.Arg703Gly)
Gene: MST1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_020998.4:c.2107C>G MANE Select NP_066278.3:p.Arg703Gly
ENST00000449682.3:c.2107C>G MANE Select ENSP00000414287.2:p.Arg703Gly
NM_001393581.1:c.2143C>G NP_001380510.1:p.Arg715Gly
NM_001393582.1:c.2050C>G NP_001380511.1:p.Arg684Gly
NM_001393583.1:c.2017C>G NP_001380512.1:p.Arg673Gly
NM_001393584.1:c.1972C>G NP_001380513.1:p.Arg658Gly
NM_001393585.1:c.1807C>G NP_001380514.1:p.Arg603Gly
NM_020998.3:c.2107C>G NP_066278.3:p.Arg703Gly
NR_146060.1:n.2060C>G
NR_146060.2:n.2771C>G
ENST00000448220.5:c.515C>G
ENST00000449682.2:c.2107C>G ENSP00000414287.2:p.Arg703Gly
ENST00000479115.5:n.2162C>G
ENST00000488350.6:n.4029C>G
ENST00000492329.5:n.1883C>G
ENST00000493836.5:n.873C>G
XM_006713166.1:c.1972C>G XP_006713229.1:p.Arg658Gly
XM_006713166.2:c.1972C>G XP_006713229.1:p.Arg658Gly
XM_011533730.1:c.2242C>G XP_011532032.1:p.Arg748Gly
XM_011533731.1:c.2149C>G XP_011532033.1:p.Arg717Gly
XM_011533732.1:c.2143C>G XP_011532034.1:p.Arg715Gly
XM_011533732.2:c.2143C>G XP_011532034.1:p.Arg715Gly
XM_011533733.1:c.*27C>G XP_011532035.1:n.*27C>G
XM_017006460.2:c.2086C>G XP_016861949.1:p.Arg696Gly
XM_017006461.2:c.2050C>G XP_016861950.1:p.Arg684Gly
XM_017006462.2:c.*27C>G XP_016861951.1:n.*27C>G
XM_017006463.2:c.*27C>G XP_016861952.1:n.*27C>G
XM_017006464.2:c.*27C>G XP_016861953.1:n.*27C>G
XR_001740149.2:n.2207C>G
XR_001740150.2:n.2204C>G
XR_001740151.2:n.2247C>G
XR_001740152.2:n.2162C>G
XR_001740153.2:n.2208C>G
XR_002959536.1:n.2162C>G
XR_427270.2:n.3039C>G
XR_427271.1:n.2990C>G
XR_427273.1:n.2895C>G
XR_427273.2:n.2166C>G
XR_427274.2:n.2940C>G
XR_940425.1:n.3035C>G
XR_940426.1:n.3075C>G
XR_940427.1:n.2940C>G
XR_940427.2:n.2211C>G