Canonical Allele Identifier: CA352882667
Gene: MST1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49684102A>C , CM000665.2:g.49684102A>C GRCh38
NC_000003.11:g.49721535A>C , CM000665.1:g.49721535A>C GRCh37
NC_000003.10:g.49696539A>C NCBI36
NG_011438.1:g.15101A>C
NG_016454.1:g.9662T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000449682.3:c.2104T>G MANE Select ENSP00000414287.2:p.Ser702Ala
ENST00000448220.5:c.512T>G
ENST00000449682.2:c.2104T>G ENSP00000414287.2:p.Ser702Ala
ENST00000479115.5:n.2159T>G
ENST00000488350.6:n.4026T>G
ENST00000492329.5:n.1880T>G
ENST00000493836.5:n.870T>G
NM_020998.3:c.2104T>G NP_066278.3:p.Ser702Ala
XM_006713166.1:c.1969T>G XP_006713229.1:p.Ser657Ala
XM_011533730.1:c.2239T>G XP_011532032.1:p.Ser747Ala
XM_011533731.1:c.2146T>G XP_011532033.1:p.Ser716Ala
XM_011533732.1:c.2140T>G XP_011532034.1:p.Ser714Ala
XM_011533733.1:c.*24T>G XP_011532035.1:n.*24T>G
XR_427270.2:n.3036T>G
XR_427271.1:n.2987T>G
XR_427273.1:n.2892T>G
XR_427274.2:n.2937T>G
XR_940425.1:n.3032T>G
XR_940426.1:n.3072T>G
XR_940427.1:n.2937T>G
NR_146060.1:n.2057T>G
XM_006713166.2:c.1969T>G XP_006713229.1:p.Ser657Ala
XM_011533732.2:c.2140T>G XP_011532034.1:p.Ser714Ala
XM_017006460.2:c.2083T>G XP_016861949.1:p.Ser695Ala
XM_017006461.2:c.2047T>G XP_016861950.1:p.Ser683Ala
XM_017006462.2:c.*24T>G XP_016861951.1:n.*24T>G
XM_017006463.2:c.*24T>G XP_016861952.1:n.*24T>G
XM_017006464.2:c.*24T>G XP_016861953.1:n.*24T>G
XR_001740149.2:n.2204T>G
XR_001740150.2:n.2201T>G
XR_001740151.2:n.2244T>G
XR_001740152.2:n.2159T>G
XR_001740153.2:n.2205T>G
XR_002959536.1:n.2159T>G
XR_427273.2:n.2163T>G
XR_940427.2:n.2208T>G
NM_001393581.1:c.2140T>G NP_001380510.1:p.Ser714Ala
NM_001393582.1:c.2047T>G NP_001380511.1:p.Ser683Ala
NM_001393583.1:c.2014T>G NP_001380512.1:p.Ser672Ala
NM_001393584.1:c.1969T>G NP_001380513.1:p.Ser657Ala
NM_001393585.1:c.1804T>G NP_001380514.1:p.Ser602Ala
NM_020998.4:c.2104T>G MANE Select NP_066278.3:p.Ser702Ala
NR_146060.2:n.2768T>G