Canonical Allele Identifier: CA2665748231

Gene: MST1

Linked Data

• gnomAD v4: 3-49684001-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684001C>T , CM000665.2:g.49684001C>T	GRCh38
NC_000003.11:g.49721434C>T , CM000665.1:g.49721434C>T	GRCh37
NC_000003.10:g.49696438C>T	NCBI36
NG_011438.1:g.15000C>T
NG_016454.1:g.9763G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*27G>A MANE Select	ENSP00000414287.2:n.*27G>A
ENST00000448220.5:c.613G>A
ENST00000449682.2:c.*27G>A	ENSP00000414287.2:n.*27G>A
ENST00000479115.5:n.2260G>A
ENST00000488350.6:n.4127G>A
ENST00000492329.5:n.1981G>A
NM_020998.3:c.*27G>A	NP_066278.3:n.*27G>A
XM_006713166.1:c.*27G>A	XP_006713229.1:n.*27G>A
XM_011533730.1:c.*27G>A	XP_011532032.1:n.*27G>A
XM_011533731.1:c.*27G>A	XP_011532033.1:n.*27G>A
XM_011533732.1:c.*27G>A	XP_011532034.1:n.*27G>A
XM_011533733.1:c.*125G>A	XP_011532035.1:n.*125G>A
XR_427270.2:n.3137G>A
XR_427271.1:n.3088G>A
XR_427273.1:n.2993G>A
XR_427274.2:n.3038G>A
XR_940425.1:n.3133G>A
XR_940426.1:n.3173G>A
XR_940427.1:n.3038G>A
NR_146060.1:n.2158G>A
XM_006713166.2:c.*27G>A	XP_006713229.1:n.*27G>A
XM_011533732.2:c.*27G>A	XP_011532034.1:n.*27G>A
XM_017006460.2:c.*27G>A	XP_016861949.1:n.*27G>A
XM_017006461.2:c.*27G>A	XP_016861950.1:n.*27G>A
XM_017006462.2:c.*125G>A	XP_016861951.1:n.*125G>A
XM_017006463.2:c.*125G>A	XP_016861952.1:n.*125G>A
XM_017006464.2:c.*125G>A	XP_016861953.1:n.*125G>A
XR_001740149.2:n.2305G>A
XR_001740150.2:n.2302G>A
XR_001740151.2:n.2345G>A
XR_001740152.2:n.2260G>A
XR_001740153.2:n.2306G>A
XR_002959536.1:n.2260G>A
XR_427273.2:n.2264G>A
XR_940427.2:n.2309G>A
NM_001393581.1:c.*27G>A	NP_001380510.1:n.*27G>A
NM_001393582.1:c.*27G>A	NP_001380511.1:n.*27G>A
NM_001393583.1:c.*27G>A	NP_001380512.1:n.*27G>A
NM_001393584.1:c.*27G>A	NP_001380513.1:n.*27G>A
NM_001393585.1:c.*27G>A	NP_001380514.1:n.*27G>A
NM_020998.4:c.*27G>A MANE Select	NP_066278.3:n.*27G>A
NR_146060.2:n.2869G>A