Canonical Allele Identifier: CA352882446

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721470T>G (hg19) ; chr3:g.49684037T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684037T>G , CM000665.2:g.49684037T>G	GRCh38
NC_000003.11:g.49721470T>G , CM000665.1:g.49721470T>G	GRCh37
NC_000003.10:g.49696474T>G	NCBI36
NG_011438.1:g.15036T>G
NG_016454.1:g.9727A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2169A>C MANE Select	ENSP00000414287.2:p.Arg723Ser
ENST00000448220.5:c.577A>C
ENST00000449682.2:c.2169A>C	ENSP00000414287.2:p.Arg723Ser
ENST00000479115.5:n.2224A>C
ENST00000488350.6:n.4091A>C
ENST00000492329.5:n.1945A>C
NM_020998.3:c.2169A>C	NP_066278.3:p.Arg723Ser
XM_006713166.1:c.2034A>C	XP_006713229.1:p.Arg678Ser
XM_011533730.1:c.2304A>C	XP_011532032.1:p.Arg768Ser
XM_011533731.1:c.2211A>C	XP_011532033.1:p.Arg737Ser
XM_011533732.1:c.2205A>C	XP_011532034.1:p.Arg735Ser
XM_011533733.1:c.*89A>C	XP_011532035.1:n.*89A>C
XR_427270.2:n.3101A>C
XR_427271.1:n.3052A>C
XR_427273.1:n.2957A>C
XR_427274.2:n.3002A>C
XR_940425.1:n.3097A>C
XR_940426.1:n.3137A>C
XR_940427.1:n.3002A>C
NR_146060.1:n.2122A>C
XM_006713166.2:c.2034A>C	XP_006713229.1:p.Arg678Ser
XM_011533732.2:c.2205A>C	XP_011532034.1:p.Arg735Ser
XM_017006460.2:c.2148A>C	XP_016861949.1:p.Arg716Ser
XM_017006461.2:c.2112A>C	XP_016861950.1:p.Arg704Ser
XM_017006462.2:c.*89A>C	XP_016861951.1:n.*89A>C
XM_017006463.2:c.*89A>C	XP_016861952.1:n.*89A>C
XM_017006464.2:c.*89A>C	XP_016861953.1:n.*89A>C
XR_001740149.2:n.2269A>C
XR_001740150.2:n.2266A>C
XR_001740151.2:n.2309A>C
XR_001740152.2:n.2224A>C
XR_001740153.2:n.2270A>C
XR_002959536.1:n.2224A>C
XR_427273.2:n.2228A>C
XR_940427.2:n.2273A>C
NM_001393581.1:c.2205A>C	NP_001380510.1:p.Arg735Ser
NM_001393582.1:c.2112A>C	NP_001380511.1:p.Arg704Ser
NM_001393583.1:c.2079A>C	NP_001380512.1:p.Arg693Ser
NM_001393584.1:c.2034A>C	NP_001380513.1:p.Arg678Ser
NM_001393585.1:c.1869A>C	NP_001380514.1:p.Arg623Ser
NM_020998.4:c.2169A>C MANE Select	NP_066278.3:p.Arg723Ser
NR_146060.2:n.2833A>C