Canonical Allele Identifier: CA433664347

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721538T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684105T>G , CM000665.2:g.49684105T>G	GRCh38
NC_000003.11:g.49721538T>G , CM000665.1:g.49721538T>G	GRCh37
NC_000003.10:g.49696542T>G	NCBI36
NG_011438.1:g.15104T>G
NG_016454.1:g.9659A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2101A>C MANE Select	ENSP00000414287.2:p.Arg701=
ENST00000448220.5:c.509A>C
ENST00000449682.2:c.2101A>C	ENSP00000414287.2:p.Arg701=
ENST00000479115.5:n.2156A>C
ENST00000488350.6:n.4023A>C
ENST00000492329.5:n.1877A>C
ENST00000493836.5:n.867A>C
NM_020998.3:c.2101A>C	NP_066278.3:p.Arg701=
XM_006713166.1:c.1966A>C	XP_006713229.1:p.Arg656=
XM_011533730.1:c.2236A>C	XP_011532032.1:p.Arg746=
XM_011533731.1:c.2143A>C	XP_011532033.1:p.Arg715=
XM_011533732.1:c.2137A>C	XP_011532034.1:p.Arg713=
XM_011533733.1:c.*21A>C	XP_011532035.1:n.*21A>C
XR_427270.2:n.3033A>C
XR_427271.1:n.2984A>C
XR_427273.1:n.2889A>C
XR_427274.2:n.2934A>C
XR_940425.1:n.3029A>C
XR_940426.1:n.3069A>C
XR_940427.1:n.2934A>C
NR_146060.1:n.2054A>C
XM_006713166.2:c.1966A>C	XP_006713229.1:p.Arg656=
XM_011533732.2:c.2137A>C	XP_011532034.1:p.Arg713=
XM_017006460.2:c.2080A>C	XP_016861949.1:p.Arg694=
XM_017006461.2:c.2044A>C	XP_016861950.1:p.Arg682=
XM_017006462.2:c.*21A>C	XP_016861951.1:n.*21A>C
XM_017006463.2:c.*21A>C	XP_016861952.1:n.*21A>C
XM_017006464.2:c.*21A>C	XP_016861953.1:n.*21A>C
XR_001740149.2:n.2201A>C
XR_001740150.2:n.2198A>C
XR_001740151.2:n.2241A>C
XR_001740152.2:n.2156A>C
XR_001740153.2:n.2202A>C
XR_002959536.1:n.2156A>C
XR_427273.2:n.2160A>C
XR_940427.2:n.2205A>C
NM_001393581.1:c.2137A>C	NP_001380510.1:p.Arg713=
NM_001393582.1:c.2044A>C	NP_001380511.1:p.Arg682=
NM_001393583.1:c.2011A>C	NP_001380512.1:p.Arg671=
NM_001393584.1:c.1966A>C	NP_001380513.1:p.Arg656=
NM_001393585.1:c.1801A>C	NP_001380514.1:p.Arg601=
NM_020998.4:c.2101A>C MANE Select	NP_066278.3:p.Arg701=
NR_146060.2:n.2765A>C