Canonical Allele Identifier: CA1363603353

Gene: MST1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49683981G= , CM000665.2:g.49683981G=	GRCh38
NC_000003.11:g.49721414G= , CM000665.1:g.49721414G=	GRCh37
NC_000003.10:g.49696418G=	NCBI36
NG_011438.1:g.14980G=
NG_016454.1:g.9783C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*47C= MANE Select	ENSP00000414287.2:n.*47C=
ENST00000448220.5:c.633C=
ENST00000449682.2:c.*47C=	ENSP00000414287.2:n.*47C=
ENST00000479115.5:n.2280C=
ENST00000488350.6:n.4147C=
ENST00000492329.5:n.2001C=
NM_020998.3:c.*47C=	NP_066278.3:n.*47C=
XM_006713166.1:c.*47C=	XP_006713229.1:n.*47C=
XM_011533730.1:c.*47C=	XP_011532032.1:n.*47C=
XM_011533731.1:c.*47C=	XP_011532033.1:n.*47C=
XM_011533732.1:c.*47C=	XP_011532034.1:n.*47C=
XM_011533733.1:c.*145C=	XP_011532035.1:n.*145C=
XR_427270.2:n.3157C=
XR_427271.1:n.3108C=
XR_427273.1:n.3013C=
XR_427274.2:n.3058C=
XR_940425.1:n.3153C=
XR_940426.1:n.3193C=
XR_940427.1:n.3058C=
NR_146060.1:n.2178C=
XM_006713166.2:c.*47C=	XP_006713229.1:n.*47C=
XM_011533732.2:c.*47C=	XP_011532034.1:n.*47C=
XM_017006460.2:c.*47C=	XP_016861949.1:n.*47C=
XM_017006461.2:c.*47C=	XP_016861950.1:n.*47C=
XM_017006462.2:c.*145C=	XP_016861951.1:n.*145C=
XM_017006463.2:c.*145C=	XP_016861952.1:n.*145C=
XM_017006464.2:c.*145C=	XP_016861953.1:n.*145C=
XR_001740149.2:n.2325C=
XR_001740150.2:n.2322C=
XR_001740151.2:n.2365C=
XR_001740152.2:n.2280C=
XR_001740153.2:n.2326C=
XR_002959536.1:n.2280C=
XR_427273.2:n.2284C=
XR_940427.2:n.2329C=
NM_001393581.1:c.*47C=	NP_001380510.1:n.*47C=
NM_001393582.1:c.*47C=	NP_001380511.1:n.*47C=
NM_001393583.1:c.*47C=	NP_001380512.1:n.*47C=
NM_001393584.1:c.*47C=	NP_001380513.1:n.*47C=
NM_001393585.1:c.*47C=	NP_001380514.1:n.*47C=
NM_020998.4:c.*47C= MANE Select	NP_066278.3:n.*47C=
NR_146060.2:n.2889C=