Canonical Allele Identifier: CA433664344

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721533G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684100G>A , CM000665.2:g.49684100G>A	GRCh38
NC_000003.11:g.49721533G>A , CM000665.1:g.49721533G>A	GRCh37
NC_000003.10:g.49696537G>A	NCBI36
NG_011438.1:g.15099G>A
NG_016454.1:g.9664C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2106C>T MANE Select	ENSP00000414287.2:p.Ser702=
ENST00000448220.5:c.514C>T
ENST00000449682.2:c.2106C>T	ENSP00000414287.2:p.Ser702=
ENST00000479115.5:n.2161C>T
ENST00000488350.6:n.4028C>T
ENST00000492329.5:n.1882C>T
ENST00000493836.5:n.872C>T
NM_020998.3:c.2106C>T	NP_066278.3:p.Ser702=
XM_006713166.1:c.1971C>T	XP_006713229.1:p.Ser657=
XM_011533730.1:c.2241C>T	XP_011532032.1:p.Ser747=
XM_011533731.1:c.2148C>T	XP_011532033.1:p.Ser716=
XM_011533732.1:c.2142C>T	XP_011532034.1:p.Ser714=
XM_011533733.1:c.*26C>T	XP_011532035.1:n.*26C>T
XR_427270.2:n.3038C>T
XR_427271.1:n.2989C>T
XR_427273.1:n.2894C>T
XR_427274.2:n.2939C>T
XR_940425.1:n.3034C>T
XR_940426.1:n.3074C>T
XR_940427.1:n.2939C>T
NR_146060.1:n.2059C>T
XM_006713166.2:c.1971C>T	XP_006713229.1:p.Ser657=
XM_011533732.2:c.2142C>T	XP_011532034.1:p.Ser714=
XM_017006460.2:c.2085C>T	XP_016861949.1:p.Ser695=
XM_017006461.2:c.2049C>T	XP_016861950.1:p.Ser683=
XM_017006462.2:c.*26C>T	XP_016861951.1:n.*26C>T
XM_017006463.2:c.*26C>T	XP_016861952.1:n.*26C>T
XM_017006464.2:c.*26C>T	XP_016861953.1:n.*26C>T
XR_001740149.2:n.2206C>T
XR_001740150.2:n.2203C>T
XR_001740151.2:n.2246C>T
XR_001740152.2:n.2161C>T
XR_001740153.2:n.2207C>T
XR_002959536.1:n.2161C>T
XR_427273.2:n.2165C>T
XR_940427.2:n.2210C>T
NM_001393581.1:c.2142C>T	NP_001380510.1:p.Ser714=
NM_001393582.1:c.2049C>T	NP_001380511.1:p.Ser683=
NM_001393583.1:c.2016C>T	NP_001380512.1:p.Ser672=
NM_001393584.1:c.1971C>T	NP_001380513.1:p.Ser657=
NM_001393585.1:c.1806C>T	NP_001380514.1:p.Ser602=
NM_020998.4:c.2106C>T MANE Select	NP_066278.3:p.Ser702=
NR_146060.2:n.2770C>T