Canonical Allele Identifier: CA352882669

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721537C>A (hg19) ; chr3:g.49684104C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684104C>A , CM000665.2:g.49684104C>A	GRCh38
NC_000003.11:g.49721537C>A , CM000665.1:g.49721537C>A	GRCh37
NC_000003.10:g.49696541C>A	NCBI36
NG_011438.1:g.15103C>A
NG_016454.1:g.9660G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000449682.3:c.2102G>T MANE Select	ENSP00000414287.2:p.Arg701Met
ENST00000448220.5:c.510G>T
ENST00000449682.2:c.2102G>T	ENSP00000414287.2:p.Arg701Met
ENST00000479115.5:n.2157G>T
ENST00000488350.6:n.4024G>T
ENST00000492329.5:n.1878G>T
ENST00000493836.5:n.868G>T
NM_020998.3:c.2102G>T	NP_066278.3:p.Arg701Met
XM_006713166.1:c.1967G>T	XP_006713229.1:p.Arg656Met
XM_011533730.1:c.2237G>T	XP_011532032.1:p.Arg746Met
XM_011533731.1:c.2144G>T	XP_011532033.1:p.Arg715Met
XM_011533732.1:c.2138G>T	XP_011532034.1:p.Arg713Met
XM_011533733.1:c.*22G>T	XP_011532035.1:n.*22G>T
XR_427270.2:n.3034G>T
XR_427271.1:n.2985G>T
XR_427273.1:n.2890G>T
XR_427274.2:n.2935G>T
XR_940425.1:n.3030G>T
XR_940426.1:n.3070G>T
XR_940427.1:n.2935G>T
NR_146060.1:n.2055G>T
XM_006713166.2:c.1967G>T	XP_006713229.1:p.Arg656Met
XM_011533732.2:c.2138G>T	XP_011532034.1:p.Arg713Met
XM_017006460.2:c.2081G>T	XP_016861949.1:p.Arg694Met
XM_017006461.2:c.2045G>T	XP_016861950.1:p.Arg682Met
XM_017006462.2:c.*22G>T	XP_016861951.1:n.*22G>T
XM_017006463.2:c.*22G>T	XP_016861952.1:n.*22G>T
XM_017006464.2:c.*22G>T	XP_016861953.1:n.*22G>T
XR_001740149.2:n.2202G>T
XR_001740150.2:n.2199G>T
XR_001740151.2:n.2242G>T
XR_001740152.2:n.2157G>T
XR_001740153.2:n.2203G>T
XR_002959536.1:n.2157G>T
XR_427273.2:n.2161G>T
XR_940427.2:n.2206G>T
NM_001393581.1:c.2138G>T	NP_001380510.1:p.Arg713Met
NM_001393582.1:c.2045G>T	NP_001380511.1:p.Arg682Met
NM_001393583.1:c.2012G>T	NP_001380512.1:p.Arg671Met
NM_001393584.1:c.1967G>T	NP_001380513.1:p.Arg656Met
NM_001393585.1:c.1802G>T	NP_001380514.1:p.Arg601Met
NM_020998.4:c.2102G>T MANE Select	NP_066278.3:p.Arg701Met
NR_146060.2:n.2766G>T