Canonical Allele Identifier: CA433664352

Gene: MST1

Linked Data

• COSMIC: COSM4118548
• MyVariant Identifiers: chr3:g.49721545T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684112T>C , CM000665.2:g.49684112T>C	GRCh38
NC_000003.11:g.49721545T>C , CM000665.1:g.49721545T>C	GRCh37
NC_000003.10:g.49696549T>C	NCBI36
NG_011438.1:g.15111T>C
NG_016454.1:g.9652A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000449682.3:c.2094A>G MANE Select	ENSP00000414287.2:p.Val698=
ENST00000448220.5:c.502A>G
ENST00000449682.2:c.2094A>G	ENSP00000414287.2:p.Val698=
ENST00000479115.5:n.2149A>G
ENST00000488350.6:n.4016A>G
ENST00000492329.5:n.1870A>G
ENST00000493836.5:n.860A>G
NM_020998.3:c.2094A>G	NP_066278.3:p.Val698=
XM_006713166.1:c.1959A>G	XP_006713229.1:p.Val653=
XM_011533730.1:c.2229A>G	XP_011532032.1:p.Val743=
XM_011533731.1:c.2136A>G	XP_011532033.1:p.Val712=
XM_011533732.1:c.2130A>G	XP_011532034.1:p.Val710=
XM_011533733.1:c.*14A>G	XP_011532035.1:n.*14A>G
XR_427270.2:n.3026A>G
XR_427271.1:n.2977A>G
XR_427273.1:n.2882A>G
XR_427274.2:n.2927A>G
XR_940425.1:n.3022A>G
XR_940426.1:n.3062A>G
XR_940427.1:n.2927A>G
NR_146060.1:n.2047A>G
XM_006713166.2:c.1959A>G	XP_006713229.1:p.Val653=
XM_011533732.2:c.2130A>G	XP_011532034.1:p.Val710=
XM_017006460.2:c.2073A>G	XP_016861949.1:p.Val691=
XM_017006461.2:c.2037A>G	XP_016861950.1:p.Val679=
XM_017006462.2:c.*14A>G	XP_016861951.1:n.*14A>G
XM_017006463.2:c.*14A>G	XP_016861952.1:n.*14A>G
XM_017006464.2:c.*14A>G	XP_016861953.1:n.*14A>G
XR_001740149.2:n.2194A>G
XR_001740150.2:n.2191A>G
XR_001740151.2:n.2234A>G
XR_001740152.2:n.2149A>G
XR_001740153.2:n.2195A>G
XR_002959536.1:n.2149A>G
XR_427273.2:n.2153A>G
XR_940427.2:n.2198A>G
NM_001393581.1:c.2130A>G	NP_001380510.1:p.Val710=
NM_001393582.1:c.2037A>G	NP_001380511.1:p.Val679=
NM_001393583.1:c.2004A>G	NP_001380512.1:p.Val668=
NM_001393584.1:c.1959A>G	NP_001380513.1:p.Val653=
NM_001393585.1:c.1794A>G	NP_001380514.1:p.Val598=
NM_020998.4:c.2094A>G MANE Select	NP_066278.3:p.Val698=
NR_146060.2:n.2758A>G