Canonical Allele Identifier: CA1363603376

Gene: MST1

Linked Data

• dbSNP Id: rs2053476590
• gnomAD v4: 3-49684021-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684021G>T , CM000665.2:g.49684021G>T	GRCh38
NC_000003.11:g.49721454G>T , CM000665.1:g.49721454G>T	GRCh37
NC_000003.10:g.49696458G>T	NCBI36
NG_011438.1:g.15020G>T
NG_016454.1:g.9743C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000449682.3:c.*7C>A MANE Select	ENSP00000414287.2:n.*7C>A
ENST00000448220.5:c.593C>A
ENST00000449682.2:c.*7C>A	ENSP00000414287.2:n.*7C>A
ENST00000479115.5:n.2240C>A
ENST00000488350.6:n.4107C>A
ENST00000492329.5:n.1961C>A
NM_020998.3:c.*7C>A	NP_066278.3:n.*7C>A
XM_006713166.1:c.*7C>A	XP_006713229.1:n.*7C>A
XM_011533730.1:c.*7C>A	XP_011532032.1:n.*7C>A
XM_011533731.1:c.*7C>A	XP_011532033.1:n.*7C>A
XM_011533732.1:c.*7C>A	XP_011532034.1:n.*7C>A
XM_011533733.1:c.*105C>A	XP_011532035.1:n.*105C>A
XR_427270.2:n.3117C>A
XR_427271.1:n.3068C>A
XR_427273.1:n.2973C>A
XR_427274.2:n.3018C>A
XR_940425.1:n.3113C>A
XR_940426.1:n.3153C>A
XR_940427.1:n.3018C>A
NR_146060.1:n.2138C>A
XM_006713166.2:c.*7C>A	XP_006713229.1:n.*7C>A
XM_011533732.2:c.*7C>A	XP_011532034.1:n.*7C>A
XM_017006460.2:c.*7C>A	XP_016861949.1:n.*7C>A
XM_017006461.2:c.*7C>A	XP_016861950.1:n.*7C>A
XM_017006462.2:c.*105C>A	XP_016861951.1:n.*105C>A
XM_017006463.2:c.*105C>A	XP_016861952.1:n.*105C>A
XM_017006464.2:c.*105C>A	XP_016861953.1:n.*105C>A
XR_001740149.2:n.2285C>A
XR_001740150.2:n.2282C>A
XR_001740151.2:n.2325C>A
XR_001740152.2:n.2240C>A
XR_001740153.2:n.2286C>A
XR_002959536.1:n.2240C>A
XR_427273.2:n.2244C>A
XR_940427.2:n.2289C>A
NM_001393581.1:c.*7C>A	NP_001380510.1:n.*7C>A
NM_001393582.1:c.*7C>A	NP_001380511.1:n.*7C>A
NM_001393583.1:c.*7C>A	NP_001380512.1:n.*7C>A
NM_001393584.1:c.*7C>A	NP_001380513.1:n.*7C>A
NM_001393585.1:c.*7C>A	NP_001380514.1:n.*7C>A
NM_020998.4:c.*7C>A MANE Select	NP_066278.3:n.*7C>A
NR_146060.2:n.2849C>A