Canonical Allele Identifier: CA352882480

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721477A>C (hg19) ; chr3:g.49684044A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684044A>C , CM000665.2:g.49684044A>C	GRCh38
NC_000003.11:g.49721477A>C , CM000665.1:g.49721477A>C	GRCh37
NC_000003.10:g.49696481A>C	NCBI36
NG_011438.1:g.15043A>C
NG_016454.1:g.9720T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2162T>G MANE Select	ENSP00000414287.2:p.Val721Gly
ENST00000448220.5:c.570T>G
ENST00000449682.2:c.2162T>G	ENSP00000414287.2:p.Val721Gly
ENST00000479115.5:n.2217T>G
ENST00000488350.6:n.4084T>G
ENST00000492329.5:n.1938T>G
NM_020998.3:c.2162T>G	NP_066278.3:p.Val721Gly
XM_006713166.1:c.2027T>G	XP_006713229.1:p.Val676Gly
XM_011533730.1:c.2297T>G	XP_011532032.1:p.Val766Gly
XM_011533731.1:c.2204T>G	XP_011532033.1:p.Val735Gly
XM_011533732.1:c.2198T>G	XP_011532034.1:p.Val733Gly
XM_011533733.1:c.*82T>G	XP_011532035.1:n.*82T>G
XR_427270.2:n.3094T>G
XR_427271.1:n.3045T>G
XR_427273.1:n.2950T>G
XR_427274.2:n.2995T>G
XR_940425.1:n.3090T>G
XR_940426.1:n.3130T>G
XR_940427.1:n.2995T>G
NR_146060.1:n.2115T>G
XM_006713166.2:c.2027T>G	XP_006713229.1:p.Val676Gly
XM_011533732.2:c.2198T>G	XP_011532034.1:p.Val733Gly
XM_017006460.2:c.2141T>G	XP_016861949.1:p.Val714Gly
XM_017006461.2:c.2105T>G	XP_016861950.1:p.Val702Gly
XM_017006462.2:c.*82T>G	XP_016861951.1:n.*82T>G
XM_017006463.2:c.*82T>G	XP_016861952.1:n.*82T>G
XM_017006464.2:c.*82T>G	XP_016861953.1:n.*82T>G
XR_001740149.2:n.2262T>G
XR_001740150.2:n.2259T>G
XR_001740151.2:n.2302T>G
XR_001740152.2:n.2217T>G
XR_001740153.2:n.2263T>G
XR_002959536.1:n.2217T>G
XR_427273.2:n.2221T>G
XR_940427.2:n.2266T>G
NM_001393581.1:c.2198T>G	NP_001380510.1:p.Val733Gly
NM_001393582.1:c.2105T>G	NP_001380511.1:p.Val702Gly
NM_001393583.1:c.2072T>G	NP_001380512.1:p.Val691Gly
NM_001393584.1:c.2027T>G	NP_001380513.1:p.Val676Gly
NM_001393585.1:c.1862T>G	NP_001380514.1:p.Val621Gly
NM_020998.4:c.2162T>G MANE Select	NP_066278.3:p.Val721Gly
NR_146060.2:n.2826T>G