Canonical Allele Identifier: CA352882461

Gene: MST1

Linked Data

• MyVariant Identifiers: chr3:g.49721473C>G (hg19) ; chr3:g.49684040C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684040C>G , CM000665.2:g.49684040C>G	GRCh38
NC_000003.11:g.49721473C>G , CM000665.1:g.49721473C>G	GRCh37
NC_000003.10:g.49696477C>G	NCBI36
NG_011438.1:g.15039C>G
NG_016454.1:g.9724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.2166G>C MANE Select	ENSP00000414287.2:p.Met722Ile
ENST00000448220.5:c.574G>C
ENST00000449682.2:c.2166G>C	ENSP00000414287.2:p.Met722Ile
ENST00000479115.5:n.2221G>C
ENST00000488350.6:n.4088G>C
ENST00000492329.5:n.1942G>C
NM_020998.3:c.2166G>C	NP_066278.3:p.Met722Ile
XM_006713166.1:c.2031G>C	XP_006713229.1:p.Met677Ile
XM_011533730.1:c.2301G>C	XP_011532032.1:p.Met767Ile
XM_011533731.1:c.2208G>C	XP_011532033.1:p.Met736Ile
XM_011533732.1:c.2202G>C	XP_011532034.1:p.Met734Ile
XM_011533733.1:c.*86G>C	XP_011532035.1:n.*86G>C
XR_427270.2:n.3098G>C
XR_427271.1:n.3049G>C
XR_427273.1:n.2954G>C
XR_427274.2:n.2999G>C
XR_940425.1:n.3094G>C
XR_940426.1:n.3134G>C
XR_940427.1:n.2999G>C
NR_146060.1:n.2119G>C
XM_006713166.2:c.2031G>C	XP_006713229.1:p.Met677Ile
XM_011533732.2:c.2202G>C	XP_011532034.1:p.Met734Ile
XM_017006460.2:c.2145G>C	XP_016861949.1:p.Met715Ile
XM_017006461.2:c.2109G>C	XP_016861950.1:p.Met703Ile
XM_017006462.2:c.*86G>C	XP_016861951.1:n.*86G>C
XM_017006463.2:c.*86G>C	XP_016861952.1:n.*86G>C
XM_017006464.2:c.*86G>C	XP_016861953.1:n.*86G>C
XR_001740149.2:n.2266G>C
XR_001740150.2:n.2263G>C
XR_001740151.2:n.2306G>C
XR_001740152.2:n.2221G>C
XR_001740153.2:n.2267G>C
XR_002959536.1:n.2221G>C
XR_427273.2:n.2225G>C
XR_940427.2:n.2270G>C
NM_001393581.1:c.2202G>C	NP_001380510.1:p.Met734Ile
NM_001393582.1:c.2109G>C	NP_001380511.1:p.Met703Ile
NM_001393583.1:c.2076G>C	NP_001380512.1:p.Met692Ile
NM_001393584.1:c.2031G>C	NP_001380513.1:p.Met677Ile
NM_001393585.1:c.1866G>C	NP_001380514.1:p.Met622Ile
NM_020998.4:c.2166G>C MANE Select	NP_066278.3:p.Met722Ile
NR_146060.2:n.2830G>C