Canonical Allele Identifier: CA352882665

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721534G>T (hg19) ; chr3:g.49684101G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684101G>T , CM000665.2:g.49684101G>T	GRCh38
NC_000003.11:g.49721534G>T , CM000665.1:g.49721534G>T	GRCh37
NC_000003.10:g.49696538G>T	NCBI36
NG_011438.1:g.15100G>T
NG_016454.1:g.9663C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2105C>A MANE Select	ENSP00000414287.2:p.Ser702Tyr
ENST00000448220.5:c.513C>A
ENST00000449682.2:c.2105C>A	ENSP00000414287.2:p.Ser702Tyr
ENST00000479115.5:n.2160C>A
ENST00000488350.6:n.4027C>A
ENST00000492329.5:n.1881C>A
ENST00000493836.5:n.871C>A
NM_020998.3:c.2105C>A	NP_066278.3:p.Ser702Tyr
XM_006713166.1:c.1970C>A	XP_006713229.1:p.Ser657Tyr
XM_011533730.1:c.2240C>A	XP_011532032.1:p.Ser747Tyr
XM_011533731.1:c.2147C>A	XP_011532033.1:p.Ser716Tyr
XM_011533732.1:c.2141C>A	XP_011532034.1:p.Ser714Tyr
XM_011533733.1:c.*25C>A	XP_011532035.1:n.*25C>A
XR_427270.2:n.3037C>A
XR_427271.1:n.2988C>A
XR_427273.1:n.2893C>A
XR_427274.2:n.2938C>A
XR_940425.1:n.3033C>A
XR_940426.1:n.3073C>A
XR_940427.1:n.2938C>A
NR_146060.1:n.2058C>A
XM_006713166.2:c.1970C>A	XP_006713229.1:p.Ser657Tyr
XM_011533732.2:c.2141C>A	XP_011532034.1:p.Ser714Tyr
XM_017006460.2:c.2084C>A	XP_016861949.1:p.Ser695Tyr
XM_017006461.2:c.2048C>A	XP_016861950.1:p.Ser683Tyr
XM_017006462.2:c.*25C>A	XP_016861951.1:n.*25C>A
XM_017006463.2:c.*25C>A	XP_016861952.1:n.*25C>A
XM_017006464.2:c.*25C>A	XP_016861953.1:n.*25C>A
XR_001740149.2:n.2205C>A
XR_001740150.2:n.2202C>A
XR_001740151.2:n.2245C>A
XR_001740152.2:n.2160C>A
XR_001740153.2:n.2206C>A
XR_002959536.1:n.2160C>A
XR_427273.2:n.2164C>A
XR_940427.2:n.2209C>A
NM_001393581.1:c.2141C>A	NP_001380510.1:p.Ser714Tyr
NM_001393582.1:c.2048C>A	NP_001380511.1:p.Ser683Tyr
NM_001393583.1:c.2015C>A	NP_001380512.1:p.Ser672Tyr
NM_001393584.1:c.1970C>A	NP_001380513.1:p.Ser657Tyr
NM_001393585.1:c.1805C>A	NP_001380514.1:p.Ser602Tyr
NM_020998.4:c.2105C>A MANE Select	NP_066278.3:p.Ser702Tyr
NR_146060.2:n.2769C>A