Canonical Allele Identifier: CA433664333

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721518G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684085G>C , CM000665.2:g.49684085G>C	GRCh38
NC_000003.11:g.49721518G>C , CM000665.1:g.49721518G>C	GRCh37
NC_000003.10:g.49696522G>C	NCBI36
NG_011438.1:g.15084G>C
NG_016454.1:g.9679C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2121C>G MANE Select	ENSP00000414287.2:p.Val707=
ENST00000448220.5:c.529C>G
ENST00000449682.2:c.2121C>G	ENSP00000414287.2:p.Val707=
ENST00000479115.5:n.2176C>G
ENST00000488350.6:n.4043C>G
ENST00000492329.5:n.1897C>G
ENST00000493836.5:n.887C>G
NM_020998.3:c.2121C>G	NP_066278.3:p.Val707=
XM_006713166.1:c.1986C>G	XP_006713229.1:p.Val662=
XM_011533730.1:c.2256C>G	XP_011532032.1:p.Val752=
XM_011533731.1:c.2163C>G	XP_011532033.1:p.Val721=
XM_011533732.1:c.2157C>G	XP_011532034.1:p.Val719=
XM_011533733.1:c.*41C>G	XP_011532035.1:n.*41C>G
XR_427270.2:n.3053C>G
XR_427271.1:n.3004C>G
XR_427273.1:n.2909C>G
XR_427274.2:n.2954C>G
XR_940425.1:n.3049C>G
XR_940426.1:n.3089C>G
XR_940427.1:n.2954C>G
NR_146060.1:n.2074C>G
XM_006713166.2:c.1986C>G	XP_006713229.1:p.Val662=
XM_011533732.2:c.2157C>G	XP_011532034.1:p.Val719=
XM_017006460.2:c.2100C>G	XP_016861949.1:p.Val700=
XM_017006461.2:c.2064C>G	XP_016861950.1:p.Val688=
XM_017006462.2:c.*41C>G	XP_016861951.1:n.*41C>G
XM_017006463.2:c.*41C>G	XP_016861952.1:n.*41C>G
XM_017006464.2:c.*41C>G	XP_016861953.1:n.*41C>G
XR_001740149.2:n.2221C>G
XR_001740150.2:n.2218C>G
XR_001740151.2:n.2261C>G
XR_001740152.2:n.2176C>G
XR_001740153.2:n.2222C>G
XR_002959536.1:n.2176C>G
XR_427273.2:n.2180C>G
XR_940427.2:n.2225C>G
NM_001393581.1:c.2157C>G	NP_001380510.1:p.Val719=
NM_001393582.1:c.2064C>G	NP_001380511.1:p.Val688=
NM_001393583.1:c.2031C>G	NP_001380512.1:p.Val677=
NM_001393584.1:c.1986C>G	NP_001380513.1:p.Val662=
NM_001393585.1:c.1821C>G	NP_001380514.1:p.Val607=
NM_020998.4:c.2121C>G MANE Select	NP_066278.3:p.Val707=
NR_146060.2:n.2785C>G