Canonical Allele Identifier: CA352882543

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721492T>A (hg19) ; chr3:g.49684059T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684059T>A , CM000665.2:g.49684059T>A	GRCh38
NC_000003.11:g.49721492T>A , CM000665.1:g.49721492T>A	GRCh37
NC_000003.10:g.49696496T>A	NCBI36
NG_011438.1:g.15058T>A
NG_016454.1:g.9705A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2147A>T MANE Select	ENSP00000414287.2:p.Asp716Val
ENST00000448220.5:c.555A>T
ENST00000449682.2:c.2147A>T	ENSP00000414287.2:p.Asp716Val
ENST00000479115.5:n.2202A>T
ENST00000488350.6:n.4069A>T
ENST00000492329.5:n.1923A>T
ENST00000493836.5:n.913A>T
NM_020998.3:c.2147A>T	NP_066278.3:p.Asp716Val
XM_006713166.1:c.2012A>T	XP_006713229.1:p.Asp671Val
XM_011533730.1:c.2282A>T	XP_011532032.1:p.Asp761Val
XM_011533731.1:c.2189A>T	XP_011532033.1:p.Asp730Val
XM_011533732.1:c.2183A>T	XP_011532034.1:p.Asp728Val
XM_011533733.1:c.*67A>T	XP_011532035.1:n.*67A>T
XR_427270.2:n.3079A>T
XR_427271.1:n.3030A>T
XR_427273.1:n.2935A>T
XR_427274.2:n.2980A>T
XR_940425.1:n.3075A>T
XR_940426.1:n.3115A>T
XR_940427.1:n.2980A>T
NR_146060.1:n.2100A>T
XM_006713166.2:c.2012A>T	XP_006713229.1:p.Asp671Val
XM_011533732.2:c.2183A>T	XP_011532034.1:p.Asp728Val
XM_017006460.2:c.2126A>T	XP_016861949.1:p.Asp709Val
XM_017006461.2:c.2090A>T	XP_016861950.1:p.Asp697Val
XM_017006462.2:c.*67A>T	XP_016861951.1:n.*67A>T
XM_017006463.2:c.*67A>T	XP_016861952.1:n.*67A>T
XM_017006464.2:c.*67A>T	XP_016861953.1:n.*67A>T
XR_001740149.2:n.2247A>T
XR_001740150.2:n.2244A>T
XR_001740151.2:n.2287A>T
XR_001740152.2:n.2202A>T
XR_001740153.2:n.2248A>T
XR_002959536.1:n.2202A>T
XR_427273.2:n.2206A>T
XR_940427.2:n.2251A>T
NM_001393581.1:c.2183A>T	NP_001380510.1:p.Asp728Val
NM_001393582.1:c.2090A>T	NP_001380511.1:p.Asp697Val
NM_001393583.1:c.2057A>T	NP_001380512.1:p.Asp686Val
NM_001393584.1:c.2012A>T	NP_001380513.1:p.Asp671Val
NM_001393585.1:c.1847A>T	NP_001380514.1:p.Asp616Val
NM_020998.4:c.2147A>T MANE Select	NP_066278.3:p.Asp716Val
NR_146060.2:n.2811A>T