Canonical Allele Identifier: CA2665748221

Gene: MST1

Linked Data

• gnomAD v4: 3-49683996-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49683996C>A , CM000665.2:g.49683996C>A	GRCh38
NC_000003.11:g.49721429C>A , CM000665.1:g.49721429C>A	GRCh37
NC_000003.10:g.49696433C>A	NCBI36
NG_011438.1:g.14995C>A
NG_016454.1:g.9768G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*32G>T MANE Select	ENSP00000414287.2:n.*32G>T
ENST00000448220.5:c.618G>T
ENST00000449682.2:c.*32G>T	ENSP00000414287.2:n.*32G>T
ENST00000479115.5:n.2265G>T
ENST00000488350.6:n.4132G>T
ENST00000492329.5:n.1986G>T
NM_020998.3:c.*32G>T	NP_066278.3:n.*32G>T
XM_006713166.1:c.*32G>T	XP_006713229.1:n.*32G>T
XM_011533730.1:c.*32G>T	XP_011532032.1:n.*32G>T
XM_011533731.1:c.*32G>T	XP_011532033.1:n.*32G>T
XM_011533732.1:c.*32G>T	XP_011532034.1:n.*32G>T
XM_011533733.1:c.*130G>T	XP_011532035.1:n.*130G>T
XR_427270.2:n.3142G>T
XR_427271.1:n.3093G>T
XR_427273.1:n.2998G>T
XR_427274.2:n.3043G>T
XR_940425.1:n.3138G>T
XR_940426.1:n.3178G>T
XR_940427.1:n.3043G>T
NR_146060.1:n.2163G>T
XM_006713166.2:c.*32G>T	XP_006713229.1:n.*32G>T
XM_011533732.2:c.*32G>T	XP_011532034.1:n.*32G>T
XM_017006460.2:c.*32G>T	XP_016861949.1:n.*32G>T
XM_017006461.2:c.*32G>T	XP_016861950.1:n.*32G>T
XM_017006462.2:c.*130G>T	XP_016861951.1:n.*130G>T
XM_017006463.2:c.*130G>T	XP_016861952.1:n.*130G>T
XM_017006464.2:c.*130G>T	XP_016861953.1:n.*130G>T
XR_001740149.2:n.2310G>T
XR_001740150.2:n.2307G>T
XR_001740151.2:n.2350G>T
XR_001740152.2:n.2265G>T
XR_001740153.2:n.2311G>T
XR_002959536.1:n.2265G>T
XR_427273.2:n.2269G>T
XR_940427.2:n.2314G>T
NM_001393581.1:c.*32G>T	NP_001380510.1:n.*32G>T
NM_001393582.1:c.*32G>T	NP_001380511.1:n.*32G>T
NM_001393583.1:c.*32G>T	NP_001380512.1:n.*32G>T
NM_001393584.1:c.*32G>T	NP_001380513.1:n.*32G>T
NM_001393585.1:c.*32G>T	NP_001380514.1:n.*32G>T
NM_020998.4:c.*32G>T MANE Select	NP_066278.3:n.*32G>T
NR_146060.2:n.2874G>T