Canonical Allele Identifier: CA2665748265

Gene: MST1

Linked Data

• gnomAD v4: 3-49684027-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684027C>G , CM000665.2:g.49684027C>G	GRCh38
NC_000003.11:g.49721460C>G , CM000665.1:g.49721460C>G	GRCh37
NC_000003.10:g.49696464C>G	NCBI36
NG_011438.1:g.15026C>G
NG_016454.1:g.9737G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*1G>C MANE Select	ENSP00000414287.2:n.*1G>C
ENST00000448220.5:c.587G>C
ENST00000449682.2:c.*1G>C	ENSP00000414287.2:n.*1G>C
ENST00000479115.5:n.2234G>C
ENST00000488350.6:n.4101G>C
ENST00000492329.5:n.1955G>C
NM_020998.3:c.*1G>C	NP_066278.3:n.*1G>C
XM_006713166.1:c.*1G>C	XP_006713229.1:n.*1G>C
XM_011533730.1:c.*1G>C	XP_011532032.1:n.*1G>C
XM_011533731.1:c.*1G>C	XP_011532033.1:n.*1G>C
XM_011533732.1:c.*1G>C	XP_011532034.1:n.*1G>C
XM_011533733.1:c.*99G>C	XP_011532035.1:n.*99G>C
XR_427270.2:n.3111G>C
XR_427271.1:n.3062G>C
XR_427273.1:n.2967G>C
XR_427274.2:n.3012G>C
XR_940425.1:n.3107G>C
XR_940426.1:n.3147G>C
XR_940427.1:n.3012G>C
NR_146060.1:n.2132G>C
XM_006713166.2:c.*1G>C	XP_006713229.1:n.*1G>C
XM_011533732.2:c.*1G>C	XP_011532034.1:n.*1G>C
XM_017006460.2:c.*1G>C	XP_016861949.1:n.*1G>C
XM_017006461.2:c.*1G>C	XP_016861950.1:n.*1G>C
XM_017006462.2:c.*99G>C	XP_016861951.1:n.*99G>C
XM_017006463.2:c.*99G>C	XP_016861952.1:n.*99G>C
XM_017006464.2:c.*99G>C	XP_016861953.1:n.*99G>C
XR_001740149.2:n.2279G>C
XR_001740150.2:n.2276G>C
XR_001740151.2:n.2319G>C
XR_001740152.2:n.2234G>C
XR_001740153.2:n.2280G>C
XR_002959536.1:n.2234G>C
XR_427273.2:n.2238G>C
XR_940427.2:n.2283G>C
NM_001393581.1:c.*1G>C	NP_001380510.1:n.*1G>C
NM_001393582.1:c.*1G>C	NP_001380511.1:n.*1G>C
NM_001393583.1:c.*1G>C	NP_001380512.1:n.*1G>C
NM_001393584.1:c.*1G>C	NP_001380513.1:n.*1G>C
NM_001393585.1:c.*1G>C	NP_001380514.1:n.*1G>C
NM_020998.4:c.*1G>C MANE Select	NP_066278.3:n.*1G>C
NR_146060.2:n.2843G>C