Canonical Allele Identifier: CA1363603359

Gene: MST1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49683998_49683999delinsTC , CM000665.2:g.49683998_49683999delinsTC	GRCh38
NC_000003.11:g.49721431_49721432delinsTC , CM000665.1:g.49721431_49721432delinsTC	GRCh37
NC_000003.10:g.49696435_49696436delinsTC	NCBI36
NG_011438.1:g.14997_14998delinsTC
NG_016454.1:g.9765_9766delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*29_*30delinsGA MANE Select	ENSP00000414287.2:n.*29_*30delinsGA
ENST00000448220.5:c.615_616delinsGA
ENST00000449682.2:c.*29_*30delinsGA	ENSP00000414287.2:n.*29_*30delinsGA
ENST00000479115.5:n.2262_2263delinsGA
ENST00000488350.6:n.4129_4130delinsGA
ENST00000492329.5:n.1983_1984delinsGA
NM_020998.3:c.*29_*30delinsGA	NP_066278.3:n.*29_*30delinsGA
XM_006713166.1:c.*29_*30delinsGA	XP_006713229.1:n.*29_*30delinsGA
XM_011533730.1:c.*29_*30delinsGA	XP_011532032.1:n.*29_*30delinsGA
XM_011533731.1:c.*29_*30delinsGA	XP_011532033.1:n.*29_*30delinsGA
XM_011533732.1:c.*29_*30delinsGA	XP_011532034.1:n.*29_*30delinsGA
XM_011533733.1:c.*127_*128delinsGA	XP_011532035.1:n.*127_*128delinsGA
XR_427270.2:n.3139_3140delinsGA
XR_427271.1:n.3090_3091delinsGA
XR_427273.1:n.2995_2996delinsGA
XR_427274.2:n.3040_3041delinsGA
XR_940425.1:n.3135_3136delinsGA
XR_940426.1:n.3175_3176delinsGA
XR_940427.1:n.3040_3041delinsGA
NR_146060.1:n.2160_2161delinsGA
XM_006713166.2:c.*29_*30delinsGA	XP_006713229.1:n.*29_*30delinsGA
XM_011533732.2:c.*29_*30delinsGA	XP_011532034.1:n.*29_*30delinsGA
XM_017006460.2:c.*29_*30delinsGA	XP_016861949.1:n.*29_*30delinsGA
XM_017006461.2:c.*29_*30delinsGA	XP_016861950.1:n.*29_*30delinsGA
XM_017006462.2:c.*127_*128delinsGA	XP_016861951.1:n.*127_*128delinsGA
XM_017006463.2:c.*127_*128delinsGA	XP_016861952.1:n.*127_*128delinsGA
XM_017006464.2:c.*127_*128delinsGA	XP_016861953.1:n.*127_*128delinsGA
XR_001740149.2:n.2307_2308delinsGA
XR_001740150.2:n.2304_2305delinsGA
XR_001740151.2:n.2347_2348delinsGA
XR_001740152.2:n.2262_2263delinsGA
XR_001740153.2:n.2308_2309delinsGA
XR_002959536.1:n.2262_2263delinsGA
XR_427273.2:n.2266_2267delinsGA
XR_940427.2:n.2311_2312delinsGA
NM_001393581.1:c.*29_*30delinsGA	NP_001380510.1:n.*29_*30delinsGA
NM_001393582.1:c.*29_*30delinsGA	NP_001380511.1:n.*29_*30delinsGA
NM_001393583.1:c.*29_*30delinsGA	NP_001380512.1:n.*29_*30delinsGA
NM_001393584.1:c.*29_*30delinsGA	NP_001380513.1:n.*29_*30delinsGA
NM_001393585.1:c.*29_*30delinsGA	NP_001380514.1:n.*29_*30delinsGA
NM_020998.4:c.*29_*30delinsGA MANE Select	NP_066278.3:n.*29_*30delinsGA
NR_146060.2:n.2871_2872delinsGA