Canonical Allele Identifier: CA2665748212

Gene: MST1

Linked Data

• gnomAD v4: 3-49683983-CAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49683987_49683989del , CM000665.2:g.49683987_49683989del	GRCh38
NC_000003.11:g.49721420_49721422del , CM000665.1:g.49721420_49721422del	GRCh37
NC_000003.10:g.49696424_49696426del	NCBI36
NG_011438.1:g.14986_14988del
NG_016454.1:g.9778_9780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*42_*44del MANE Select	ENSP00000414287.2:n.*42_*44del
ENST00000448220.5:c.628_630del
ENST00000449682.2:c.*42_*44del	ENSP00000414287.2:n.*42_*44del
ENST00000479115.5:n.2275_2277del
ENST00000488350.6:n.4142_4144del
ENST00000492329.5:n.1996_1998del
NM_020998.3:c.*42_*44del	NP_066278.3:n.*42_*44del
XM_006713166.1:c.*42_*44del	XP_006713229.1:n.*42_*44del
XM_011533730.1:c.*42_*44del	XP_011532032.1:n.*42_*44del
XM_011533731.1:c.*42_*44del	XP_011532033.1:n.*42_*44del
XM_011533732.1:c.*42_*44del	XP_011532034.1:n.*42_*44del
XM_011533733.1:c.*140_*142del	XP_011532035.1:n.*140_*142del
XR_427270.2:n.3152_3154del
XR_427271.1:n.3103_3105del
XR_427273.1:n.3008_3010del
XR_427274.2:n.3053_3055del
XR_940425.1:n.3148_3150del
XR_940426.1:n.3188_3190del
XR_940427.1:n.3053_3055del
NR_146060.1:n.2173_2175del
XM_006713166.2:c.*42_*44del	XP_006713229.1:n.*42_*44del
XM_011533732.2:c.*42_*44del	XP_011532034.1:n.*42_*44del
XM_017006460.2:c.*42_*44del	XP_016861949.1:n.*42_*44del
XM_017006461.2:c.*42_*44del	XP_016861950.1:n.*42_*44del
XM_017006462.2:c.*140_*142del	XP_016861951.1:n.*140_*142del
XM_017006463.2:c.*140_*142del	XP_016861952.1:n.*140_*142del
XM_017006464.2:c.*140_*142del	XP_016861953.1:n.*140_*142del
XR_001740149.2:n.2320_2322del
XR_001740150.2:n.2317_2319del
XR_001740151.2:n.2360_2362del
XR_001740152.2:n.2275_2277del
XR_001740153.2:n.2321_2323del
XR_002959536.1:n.2275_2277del
XR_427273.2:n.2279_2281del
XR_940427.2:n.2324_2326del
NM_001393581.1:c.*42_*44del	NP_001380510.1:n.*42_*44del
NM_001393582.1:c.*42_*44del	NP_001380511.1:n.*42_*44del
NM_001393583.1:c.*42_*44del	NP_001380512.1:n.*42_*44del
NM_001393584.1:c.*42_*44del	NP_001380513.1:n.*42_*44del
NM_001393585.1:c.*42_*44del	NP_001380514.1:n.*42_*44del
NM_020998.4:c.*42_*44del MANE Select	NP_066278.3:n.*42_*44del
NR_146060.2:n.2884_2886del