Canonical Allele Identifier: CA433664325

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721503A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684070A>T , CM000665.2:g.49684070A>T	GRCh38
NC_000003.11:g.49721503A>T , CM000665.1:g.49721503A>T	GRCh37
NC_000003.10:g.49696507A>T	NCBI36
NG_011438.1:g.15069A>T
NG_016454.1:g.9694T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2136T>A MANE Select	ENSP00000414287.2:p.Ser712=
ENST00000448220.5:c.544T>A
ENST00000449682.2:c.2136T>A	ENSP00000414287.2:p.Ser712=
ENST00000479115.5:n.2191T>A
ENST00000488350.6:n.4058T>A
ENST00000492329.5:n.1912T>A
ENST00000493836.5:n.902T>A
NM_020998.3:c.2136T>A	NP_066278.3:p.Ser712=
XM_006713166.1:c.2001T>A	XP_006713229.1:p.Ser667=
XM_011533730.1:c.2271T>A	XP_011532032.1:p.Ser757=
XM_011533731.1:c.2178T>A	XP_011532033.1:p.Ser726=
XM_011533732.1:c.2172T>A	XP_011532034.1:p.Ser724=
XM_011533733.1:c.*56T>A	XP_011532035.1:n.*56T>A
XR_427270.2:n.3068T>A
XR_427271.1:n.3019T>A
XR_427273.1:n.2924T>A
XR_427274.2:n.2969T>A
XR_940425.1:n.3064T>A
XR_940426.1:n.3104T>A
XR_940427.1:n.2969T>A
NR_146060.1:n.2089T>A
XM_006713166.2:c.2001T>A	XP_006713229.1:p.Ser667=
XM_011533732.2:c.2172T>A	XP_011532034.1:p.Ser724=
XM_017006460.2:c.2115T>A	XP_016861949.1:p.Ser705=
XM_017006461.2:c.2079T>A	XP_016861950.1:p.Ser693=
XM_017006462.2:c.*56T>A	XP_016861951.1:n.*56T>A
XM_017006463.2:c.*56T>A	XP_016861952.1:n.*56T>A
XM_017006464.2:c.*56T>A	XP_016861953.1:n.*56T>A
XR_001740149.2:n.2236T>A
XR_001740150.2:n.2233T>A
XR_001740151.2:n.2276T>A
XR_001740152.2:n.2191T>A
XR_001740153.2:n.2237T>A
XR_002959536.1:n.2191T>A
XR_427273.2:n.2195T>A
XR_940427.2:n.2240T>A
NM_001393581.1:c.2172T>A	NP_001380510.1:p.Ser724=
NM_001393582.1:c.2079T>A	NP_001380511.1:p.Ser693=
NM_001393583.1:c.2046T>A	NP_001380512.1:p.Ser682=
NM_001393584.1:c.2001T>A	NP_001380513.1:p.Ser667=
NM_001393585.1:c.1836T>A	NP_001380514.1:p.Ser612=
NM_020998.4:c.2136T>A MANE Select	NP_066278.3:p.Ser712=
NR_146060.2:n.2800T>A