Canonical Allele Identifier: CA433664306

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721467C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684034C>G , CM000665.2:g.49684034C>G	GRCh38
NC_000003.11:g.49721467C>G , CM000665.1:g.49721467C>G	GRCh37
NC_000003.10:g.49696471C>G	NCBI36
NG_011438.1:g.15033C>G
NG_016454.1:g.9730G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2172G>C MANE Select	ENSP00000414287.2:p.Leu724=
ENST00000448220.5:c.580G>C
ENST00000449682.2:c.2172G>C	ENSP00000414287.2:p.Leu724=
ENST00000479115.5:n.2227G>C
ENST00000488350.6:n.4094G>C
ENST00000492329.5:n.1948G>C
NM_020998.3:c.2172G>C	NP_066278.3:p.Leu724=
XM_006713166.1:c.2037G>C	XP_006713229.1:p.Leu679=
XM_011533730.1:c.2307G>C	XP_011532032.1:p.Leu769=
XM_011533731.1:c.2214G>C	XP_011532033.1:p.Leu738=
XM_011533732.1:c.2208G>C	XP_011532034.1:p.Leu736=
XM_011533733.1:c.*92G>C	XP_011532035.1:n.*92G>C
XR_427270.2:n.3104G>C
XR_427271.1:n.3055G>C
XR_427273.1:n.2960G>C
XR_427274.2:n.3005G>C
XR_940425.1:n.3100G>C
XR_940426.1:n.3140G>C
XR_940427.1:n.3005G>C
NR_146060.1:n.2125G>C
XM_006713166.2:c.2037G>C	XP_006713229.1:p.Leu679=
XM_011533732.2:c.2208G>C	XP_011532034.1:p.Leu736=
XM_017006460.2:c.2151G>C	XP_016861949.1:p.Leu717=
XM_017006461.2:c.2115G>C	XP_016861950.1:p.Leu705=
XM_017006462.2:c.*92G>C	XP_016861951.1:n.*92G>C
XM_017006463.2:c.*92G>C	XP_016861952.1:n.*92G>C
XM_017006464.2:c.*92G>C	XP_016861953.1:n.*92G>C
XR_001740149.2:n.2272G>C
XR_001740150.2:n.2269G>C
XR_001740151.2:n.2312G>C
XR_001740152.2:n.2227G>C
XR_001740153.2:n.2273G>C
XR_002959536.1:n.2227G>C
XR_427273.2:n.2231G>C
XR_940427.2:n.2276G>C
NM_001393581.1:c.2208G>C	NP_001380510.1:p.Leu736=
NM_001393582.1:c.2115G>C	NP_001380511.1:p.Leu705=
NM_001393583.1:c.2082G>C	NP_001380512.1:p.Leu694=
NM_001393584.1:c.2037G>C	NP_001380513.1:p.Leu679=
NM_001393585.1:c.1872G>C	NP_001380514.1:p.Leu624=
NM_020998.4:c.2172G>C MANE Select	NP_066278.3:p.Leu724=
NR_146060.2:n.2836G>C