Canonical Allele Identifier: CA2665748214

Gene: MST1

Linked Data

• gnomAD v4: 3-49683985-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49683985A>T , CM000665.2:g.49683985A>T	GRCh38
NC_000003.11:g.49721418A>T , CM000665.1:g.49721418A>T	GRCh37
NC_000003.10:g.49696422A>T	NCBI36
NG_011438.1:g.14984A>T
NG_016454.1:g.9779T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*43T>A MANE Select	ENSP00000414287.2:n.*43T>A
ENST00000448220.5:c.629T>A
ENST00000449682.2:c.*43T>A	ENSP00000414287.2:n.*43T>A
ENST00000479115.5:n.2276T>A
ENST00000488350.6:n.4143T>A
ENST00000492329.5:n.1997T>A
NM_020998.3:c.*43T>A	NP_066278.3:n.*43T>A
XM_006713166.1:c.*43T>A	XP_006713229.1:n.*43T>A
XM_011533730.1:c.*43T>A	XP_011532032.1:n.*43T>A
XM_011533731.1:c.*43T>A	XP_011532033.1:n.*43T>A
XM_011533732.1:c.*43T>A	XP_011532034.1:n.*43T>A
XM_011533733.1:c.*141T>A	XP_011532035.1:n.*141T>A
XR_427270.2:n.3153T>A
XR_427271.1:n.3104T>A
XR_427273.1:n.3009T>A
XR_427274.2:n.3054T>A
XR_940425.1:n.3149T>A
XR_940426.1:n.3189T>A
XR_940427.1:n.3054T>A
NR_146060.1:n.2174T>A
XM_006713166.2:c.*43T>A	XP_006713229.1:n.*43T>A
XM_011533732.2:c.*43T>A	XP_011532034.1:n.*43T>A
XM_017006460.2:c.*43T>A	XP_016861949.1:n.*43T>A
XM_017006461.2:c.*43T>A	XP_016861950.1:n.*43T>A
XM_017006462.2:c.*141T>A	XP_016861951.1:n.*141T>A
XM_017006463.2:c.*141T>A	XP_016861952.1:n.*141T>A
XM_017006464.2:c.*141T>A	XP_016861953.1:n.*141T>A
XR_001740149.2:n.2321T>A
XR_001740150.2:n.2318T>A
XR_001740151.2:n.2361T>A
XR_001740152.2:n.2276T>A
XR_001740153.2:n.2322T>A
XR_002959536.1:n.2276T>A
XR_427273.2:n.2280T>A
XR_940427.2:n.2325T>A
NM_001393581.1:c.*43T>A	NP_001380510.1:n.*43T>A
NM_001393582.1:c.*43T>A	NP_001380511.1:n.*43T>A
NM_001393583.1:c.*43T>A	NP_001380512.1:n.*43T>A
NM_001393584.1:c.*43T>A	NP_001380513.1:n.*43T>A
NM_001393585.1:c.*43T>A	NP_001380514.1:n.*43T>A
NM_020998.4:c.*43T>A MANE Select	NP_066278.3:n.*43T>A
NR_146060.2:n.2885T>A