Canonical Allele Identifier: CA1363603365

Gene: MST1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684008A= , CM000665.2:g.49684008A=	GRCh38
NC_000003.11:g.49721441A= , CM000665.1:g.49721441A=	GRCh37
NC_000003.10:g.49696445A=	NCBI36
NG_011438.1:g.15007A=
NG_016454.1:g.9756T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*20T= MANE Select	ENSP00000414287.2:n.*20T=
ENST00000448220.5:c.606T=
ENST00000449682.2:c.*20T=	ENSP00000414287.2:n.*20T=
ENST00000479115.5:n.2253T=
ENST00000488350.6:n.4120T=
ENST00000492329.5:n.1974T=
NM_020998.3:c.*20T=	NP_066278.3:n.*20T=
XM_006713166.1:c.*20T=	XP_006713229.1:n.*20T=
XM_011533730.1:c.*20T=	XP_011532032.1:n.*20T=
XM_011533731.1:c.*20T=	XP_011532033.1:n.*20T=
XM_011533732.1:c.*20T=	XP_011532034.1:n.*20T=
XM_011533733.1:c.*118T=	XP_011532035.1:n.*118T=
XR_427270.2:n.3130T=
XR_427271.1:n.3081T=
XR_427273.1:n.2986T=
XR_427274.2:n.3031T=
XR_940425.1:n.3126T=
XR_940426.1:n.3166T=
XR_940427.1:n.3031T=
NR_146060.1:n.2151T=
XM_006713166.2:c.*20T=	XP_006713229.1:n.*20T=
XM_011533732.2:c.*20T=	XP_011532034.1:n.*20T=
XM_017006460.2:c.*20T=	XP_016861949.1:n.*20T=
XM_017006461.2:c.*20T=	XP_016861950.1:n.*20T=
XM_017006462.2:c.*118T=	XP_016861951.1:n.*118T=
XM_017006463.2:c.*118T=	XP_016861952.1:n.*118T=
XM_017006464.2:c.*118T=	XP_016861953.1:n.*118T=
XR_001740149.2:n.2298T=
XR_001740150.2:n.2295T=
XR_001740151.2:n.2338T=
XR_001740152.2:n.2253T=
XR_001740153.2:n.2299T=
XR_002959536.1:n.2253T=
XR_427273.2:n.2257T=
XR_940427.2:n.2302T=
NM_001393581.1:c.*20T=	NP_001380510.1:n.*20T=
NM_001393582.1:c.*20T=	NP_001380511.1:n.*20T=
NM_001393583.1:c.*20T=	NP_001380512.1:n.*20T=
NM_001393584.1:c.*20T=	NP_001380513.1:n.*20T=
NM_001393585.1:c.*20T=	NP_001380514.1:n.*20T=
NM_020998.4:c.*20T= MANE Select	NP_066278.3:n.*20T=
NR_146060.2:n.2862T=