Canonical Allele Identifier: CA352882668

Gene: MST1

Linked Data

• dbSNP Id: rs774684470
• MyVariant Identifiers: chr3:g.49721536C>G (hg19) ; chr3:g.49684103C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684103C>G , CM000665.2:g.49684103C>G	GRCh38
NC_000003.11:g.49721536C>G , CM000665.1:g.49721536C>G	GRCh37
NC_000003.10:g.49696540C>G	NCBI36
NG_011438.1:g.15102C>G
NG_016454.1:g.9661G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2103G>C MANE Select	ENSP00000414287.2:p.Arg701Ser
ENST00000448220.5:c.511G>C
ENST00000449682.2:c.2103G>C	ENSP00000414287.2:p.Arg701Ser
ENST00000479115.5:n.2158G>C
ENST00000488350.6:n.4025G>C
ENST00000492329.5:n.1879G>C
ENST00000493836.5:n.869G>C
NM_020998.3:c.2103G>C	NP_066278.3:p.Arg701Ser
XM_006713166.1:c.1968G>C	XP_006713229.1:p.Arg656Ser
XM_011533730.1:c.2238G>C	XP_011532032.1:p.Arg746Ser
XM_011533731.1:c.2145G>C	XP_011532033.1:p.Arg715Ser
XM_011533732.1:c.2139G>C	XP_011532034.1:p.Arg713Ser
XM_011533733.1:c.*23G>C	XP_011532035.1:n.*23G>C
XR_427270.2:n.3035G>C
XR_427271.1:n.2986G>C
XR_427273.1:n.2891G>C
XR_427274.2:n.2936G>C
XR_940425.1:n.3031G>C
XR_940426.1:n.3071G>C
XR_940427.1:n.2936G>C
NR_146060.1:n.2056G>C
XM_006713166.2:c.1968G>C	XP_006713229.1:p.Arg656Ser
XM_011533732.2:c.2139G>C	XP_011532034.1:p.Arg713Ser
XM_017006460.2:c.2082G>C	XP_016861949.1:p.Arg694Ser
XM_017006461.2:c.2046G>C	XP_016861950.1:p.Arg682Ser
XM_017006462.2:c.*23G>C	XP_016861951.1:n.*23G>C
XM_017006463.2:c.*23G>C	XP_016861952.1:n.*23G>C
XM_017006464.2:c.*23G>C	XP_016861953.1:n.*23G>C
XR_001740149.2:n.2203G>C
XR_001740150.2:n.2200G>C
XR_001740151.2:n.2243G>C
XR_001740152.2:n.2158G>C
XR_001740153.2:n.2204G>C
XR_002959536.1:n.2158G>C
XR_427273.2:n.2162G>C
XR_940427.2:n.2207G>C
NM_001393581.1:c.2139G>C	NP_001380510.1:p.Arg713Ser
NM_001393582.1:c.2046G>C	NP_001380511.1:p.Arg682Ser
NM_001393583.1:c.2013G>C	NP_001380512.1:p.Arg671Ser
NM_001393584.1:c.1968G>C	NP_001380513.1:p.Arg656Ser
NM_001393585.1:c.1803G>C	NP_001380514.1:p.Arg601Ser
NM_020998.4:c.2103G>C MANE Select	NP_066278.3:p.Arg701Ser
NR_146060.2:n.2767G>C