Canonical Allele Identifier: CA2665748239

Gene: MST1

Linked Data

• gnomAD v4: 3-49684009-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684009T>C , CM000665.2:g.49684009T>C	GRCh38
NC_000003.11:g.49721442T>C , CM000665.1:g.49721442T>C	GRCh37
NC_000003.10:g.49696446T>C	NCBI36
NG_011438.1:g.15008T>C
NG_016454.1:g.9755A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*19A>G MANE Select	ENSP00000414287.2:n.*19A>G
ENST00000448220.5:c.605A>G
ENST00000449682.2:c.*19A>G	ENSP00000414287.2:n.*19A>G
ENST00000479115.5:n.2252A>G
ENST00000488350.6:n.4119A>G
ENST00000492329.5:n.1973A>G
NM_020998.3:c.*19A>G	NP_066278.3:n.*19A>G
XM_006713166.1:c.*19A>G	XP_006713229.1:n.*19A>G
XM_011533730.1:c.*19A>G	XP_011532032.1:n.*19A>G
XM_011533731.1:c.*19A>G	XP_011532033.1:n.*19A>G
XM_011533732.1:c.*19A>G	XP_011532034.1:n.*19A>G
XM_011533733.1:c.*117A>G	XP_011532035.1:n.*117A>G
XR_427270.2:n.3129A>G
XR_427271.1:n.3080A>G
XR_427273.1:n.2985A>G
XR_427274.2:n.3030A>G
XR_940425.1:n.3125A>G
XR_940426.1:n.3165A>G
XR_940427.1:n.3030A>G
NR_146060.1:n.2150A>G
XM_006713166.2:c.*19A>G	XP_006713229.1:n.*19A>G
XM_011533732.2:c.*19A>G	XP_011532034.1:n.*19A>G
XM_017006460.2:c.*19A>G	XP_016861949.1:n.*19A>G
XM_017006461.2:c.*19A>G	XP_016861950.1:n.*19A>G
XM_017006462.2:c.*117A>G	XP_016861951.1:n.*117A>G
XM_017006463.2:c.*117A>G	XP_016861952.1:n.*117A>G
XM_017006464.2:c.*117A>G	XP_016861953.1:n.*117A>G
XR_001740149.2:n.2297A>G
XR_001740150.2:n.2294A>G
XR_001740151.2:n.2337A>G
XR_001740152.2:n.2252A>G
XR_001740153.2:n.2298A>G
XR_002959536.1:n.2252A>G
XR_427273.2:n.2256A>G
XR_940427.2:n.2301A>G
NM_001393581.1:c.*19A>G	NP_001380510.1:n.*19A>G
NM_001393582.1:c.*19A>G	NP_001380511.1:n.*19A>G
NM_001393583.1:c.*19A>G	NP_001380512.1:n.*19A>G
NM_001393584.1:c.*19A>G	NP_001380513.1:n.*19A>G
NM_001393585.1:c.*19A>G	NP_001380514.1:n.*19A>G
NM_020998.4:c.*19A>G MANE Select	NP_066278.3:n.*19A>G
NR_146060.2:n.2861A>G