Canonical Allele Identifier: CA352882571

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721498A>C (hg19) ; chr3:g.49684065A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684065A>C , CM000665.2:g.49684065A>C	GRCh38
NC_000003.11:g.49721498A>C , CM000665.1:g.49721498A>C	GRCh37
NC_000003.10:g.49696502A>C	NCBI36
NG_011438.1:g.15064A>C
NG_016454.1:g.9699T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2141T>G MANE Select	ENSP00000414287.2:p.Phe714Cys
ENST00000448220.5:c.549T>G
ENST00000449682.2:c.2141T>G	ENSP00000414287.2:p.Phe714Cys
ENST00000479115.5:n.2196T>G
ENST00000488350.6:n.4063T>G
ENST00000492329.5:n.1917T>G
ENST00000493836.5:n.907T>G
NM_020998.3:c.2141T>G	NP_066278.3:p.Phe714Cys
XM_006713166.1:c.2006T>G	XP_006713229.1:p.Phe669Cys
XM_011533730.1:c.2276T>G	XP_011532032.1:p.Phe759Cys
XM_011533731.1:c.2183T>G	XP_011532033.1:p.Phe728Cys
XM_011533732.1:c.2177T>G	XP_011532034.1:p.Phe726Cys
XM_011533733.1:c.*61T>G	XP_011532035.1:n.*61T>G
XR_427270.2:n.3073T>G
XR_427271.1:n.3024T>G
XR_427273.1:n.2929T>G
XR_427274.2:n.2974T>G
XR_940425.1:n.3069T>G
XR_940426.1:n.3109T>G
XR_940427.1:n.2974T>G
NR_146060.1:n.2094T>G
XM_006713166.2:c.2006T>G	XP_006713229.1:p.Phe669Cys
XM_011533732.2:c.2177T>G	XP_011532034.1:p.Phe726Cys
XM_017006460.2:c.2120T>G	XP_016861949.1:p.Phe707Cys
XM_017006461.2:c.2084T>G	XP_016861950.1:p.Phe695Cys
XM_017006462.2:c.*61T>G	XP_016861951.1:n.*61T>G
XM_017006463.2:c.*61T>G	XP_016861952.1:n.*61T>G
XM_017006464.2:c.*61T>G	XP_016861953.1:n.*61T>G
XR_001740149.2:n.2241T>G
XR_001740150.2:n.2238T>G
XR_001740151.2:n.2281T>G
XR_001740152.2:n.2196T>G
XR_001740153.2:n.2242T>G
XR_002959536.1:n.2196T>G
XR_427273.2:n.2200T>G
XR_940427.2:n.2245T>G
NM_001393581.1:c.2177T>G	NP_001380510.1:p.Phe726Cys
NM_001393582.1:c.2084T>G	NP_001380511.1:p.Phe695Cys
NM_001393583.1:c.2051T>G	NP_001380512.1:p.Phe684Cys
NM_001393584.1:c.2006T>G	NP_001380513.1:p.Phe669Cys
NM_001393585.1:c.1841T>G	NP_001380514.1:p.Phe614Cys
NM_020998.4:c.2141T>G MANE Select	NP_066278.3:p.Phe714Cys
NR_146060.2:n.2805T>G