Canonical Allele Identifier: CA433664308

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721469G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684036G>A , CM000665.2:g.49684036G>A	GRCh38
NC_000003.11:g.49721469G>A , CM000665.1:g.49721469G>A	GRCh37
NC_000003.10:g.49696473G>A	NCBI36
NG_011438.1:g.15035G>A
NG_016454.1:g.9728C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2170C>T MANE Select	ENSP00000414287.2:p.Leu724=
ENST00000448220.5:c.578C>T
ENST00000449682.2:c.2170C>T	ENSP00000414287.2:p.Leu724=
ENST00000479115.5:n.2225C>T
ENST00000488350.6:n.4092C>T
ENST00000492329.5:n.1946C>T
NM_020998.3:c.2170C>T	NP_066278.3:p.Leu724=
XM_006713166.1:c.2035C>T	XP_006713229.1:p.Leu679=
XM_011533730.1:c.2305C>T	XP_011532032.1:p.Leu769=
XM_011533731.1:c.2212C>T	XP_011532033.1:p.Leu738=
XM_011533732.1:c.2206C>T	XP_011532034.1:p.Leu736=
XM_011533733.1:c.*90C>T	XP_011532035.1:n.*90C>T
XR_427270.2:n.3102C>T
XR_427271.1:n.3053C>T
XR_427273.1:n.2958C>T
XR_427274.2:n.3003C>T
XR_940425.1:n.3098C>T
XR_940426.1:n.3138C>T
XR_940427.1:n.3003C>T
NR_146060.1:n.2123C>T
XM_006713166.2:c.2035C>T	XP_006713229.1:p.Leu679=
XM_011533732.2:c.2206C>T	XP_011532034.1:p.Leu736=
XM_017006460.2:c.2149C>T	XP_016861949.1:p.Leu717=
XM_017006461.2:c.2113C>T	XP_016861950.1:p.Leu705=
XM_017006462.2:c.*90C>T	XP_016861951.1:n.*90C>T
XM_017006463.2:c.*90C>T	XP_016861952.1:n.*90C>T
XM_017006464.2:c.*90C>T	XP_016861953.1:n.*90C>T
XR_001740149.2:n.2270C>T
XR_001740150.2:n.2267C>T
XR_001740151.2:n.2310C>T
XR_001740152.2:n.2225C>T
XR_001740153.2:n.2271C>T
XR_002959536.1:n.2225C>T
XR_427273.2:n.2229C>T
XR_940427.2:n.2274C>T
NM_001393581.1:c.2206C>T	NP_001380510.1:p.Leu736=
NM_001393582.1:c.2113C>T	NP_001380511.1:p.Leu705=
NM_001393583.1:c.2080C>T	NP_001380512.1:p.Leu694=
NM_001393584.1:c.2035C>T	NP_001380513.1:p.Leu679=
NM_001393585.1:c.1870C>T	NP_001380514.1:p.Leu624=
NM_020998.4:c.2170C>T MANE Select	NP_066278.3:p.Leu724=
NR_146060.2:n.2834C>T