Canonical Allele Identifier: CA364716961

Gene: MTO1

Linked Data

• MyVariant Identifiers: chr6:g.74191800G>C (hg19) ; chr6:g.73482077G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73482077G>C , CM000668.2:g.73482077G>C	GRCh38
NC_000006.11:g.74191800G>C , CM000668.1:g.74191800G>C	GRCh37
NC_000006.10:g.74248521G>C	NCBI36
NG_032856.1:g.25347G>C
NG_032856.2:g.25347G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442897.7:c.*429G>C	ENSP00000396529.2:n.*429G>C
ENST00000445187.6:c.*440G>C	ENSP00000407580.2:n.*440G>C
ENST00000487960.2:n.1380G>C
ENST00000498286.6:c.1298G>C MANE Select	ENSP00000419561.2:p.Ser433Thr
ENST00000521156.6:c.1076G>C	ENSP00000428863.2:p.Ser359Thr
ENST00000522205.6:c.*841G>C	ENSP00000428903.2:n.*841G>C
ENST00000523763.2:c.1298G>C	ENSP00000429595.2:p.Ser433Thr
ENST00000524046.2:c.*891G>C	ENSP00000430660.2:n.*891G>C
ENST00000679352.1:c.*670G>C	ENSP00000505776.1:n.*670G>C
ENST00000679364.1:c.*440G>C	ENSP00000505626.1:n.*440G>C
ENST00000679411.1:c.*1093G>C	ENSP00000506532.1:n.*1093G>C
ENST00000679418.1:c.*852G>C	ENSP00000505278.1:n.*852G>C
ENST00000679524.1:c.*552G>C	ENSP00000505038.1:n.*552G>C
ENST00000679591.1:c.1291G>C	ENSP00000505656.1:n.1291G>C
ENST00000679592.1:c.*1112G>C	ENSP00000505736.1:n.*1112G>C
ENST00000679604.1:c.*608-372G>C	ENSP00000506268.1:n.*608-372G>C
ENST00000679612.1:n.1663G>C
ENST00000679627.1:c.*142G>C	ENSP00000505373.1:n.*142G>C
ENST00000679675.1:c.1336-372G>C	ENSP00000505458.1:n.1336-372G>C
ENST00000679730.1:c.*502-372G>C	ENSP00000506698.1:n.*502-372G>C
ENST00000679808.1:c.*115G>C	ENSP00000506127.1:n.*115G>C
ENST00000679870.1:c.*852G>C	ENSP00000505401.1:n.*852G>C
ENST00000679900.1:c.*342G>C	ENSP00000505653.1:n.*342G>C
ENST00000679905.1:c.1261-372G>C	ENSP00000505787.1:n.1261-372G>C
ENST00000679947.1:c.*142G>C	ENSP00000506630.1:n.*142G>C
ENST00000679993.1:n.1377G>C
ENST00000680034.1:c.*545G>C	ENSP00000505785.1:n.*545G>C
ENST00000680131.1:c.*31G>C	ENSP00000505906.1:n.*31G>C
ENST00000680195.1:n.1495G>C
ENST00000680238.1:c.*841G>C	ENSP00000506260.1:n.*841G>C
ENST00000680266.1:n.1663G>C
ENST00000680289.1:c.*841G>C	ENSP00000505097.1:n.*841G>C
ENST00000680350.1:n.1625+1272G>C
ENST00000680405.1:n.1630G>C
ENST00000680428.1:c.*255G>C	ENSP00000506210.1:n.*255G>C
ENST00000680544.1:c.*804-372G>C	ENSP00000506702.1:n.*804-372G>C
ENST00000680563.1:c.957G>C
ENST00000680570.1:n.1674G>C
ENST00000680601.1:c.*822G>C	ENSP00000506582.1:n.*822G>C
ENST00000680609.1:c.*429G>C	ENSP00000505053.1:n.*429G>C
ENST00000680686.1:c.1076G>C	ENSP00000506609.1:p.Ser359Thr
ENST00000680758.1:c.*1063G>C	ENSP00000505192.1:n.*1063G>C
ENST00000680775.1:c.*676G>C	ENSP00000505199.1:n.*676G>C
ENST00000680794.1:c.*1045-372G>C	ENSP00000506362.1:n.*1045-372G>C
ENST00000680841.1:c.1277G>C	ENSP00000506524.1:n.1277G>C
ENST00000680875.1:c.*78-372G>C	ENSP00000506042.1:n.*78-372G>C
ENST00000680902.1:c.*269G>C	ENSP00000505813.1:n.*269G>C
ENST00000681094.1:c.*115G>C	ENSP00000505394.1:n.*115G>C
ENST00000681141.1:c.*854-372G>C	ENSP00000506035.1:n.*854-372G>C
ENST00000681165.1:c.*852G>C	ENSP00000506088.1:n.*852G>C
ENST00000681204.1:c.1298G>C	ENSP00000505819.1:p.Ser433Thr
ENST00000681212.1:n.1742-372G>C
ENST00000681254.1:c.*957G>C	ENSP00000506575.1:n.*957G>C
ENST00000681267.1:c.*78-372G>C	ENSP00000506570.1:n.*78-372G>C
ENST00000681284.1:n.1663G>C
ENST00000681294.1:c.*255G>C	ENSP00000505615.1:n.*255G>C
ENST00000681337.1:c.*115G>C	ENSP00000506108.1:n.*115G>C
ENST00000681438.1:c.*391+1272G>C	ENSP00000505135.1:n.*391+1272G>C
ENST00000681500.1:c.1016G>C	ENSP00000506439.1:p.Ser339Thr
ENST00000681509.1:c.*31G>C	ENSP00000506571.1:n.*31G>C
ENST00000681579.1:c.1039-372G>C	ENSP00000505732.1:n.1039-372G>C
ENST00000681610.1:c.1260+1272G>C	ENSP00000505229.1:n.1260+1272G>C
ENST00000681620.1:c.*105-372G>C	ENSP00000505386.1:n.*105-372G>C
ENST00000681624.1:c.*1065G>C	ENSP00000505820.1:n.*1065G>C
ENST00000681691.1:c.1298G>C	ENSP00000505613.1:p.Ser433Thr
ENST00000681705.1:c.*31G>C	ENSP00000506381.1:n.*31G>C
ENST00000681890.1:c.*31G>C	ENSP00000505751.1:n.*31G>C
ENST00000681932.1:c.*611G>C	ENSP00000505826.1:n.*611G>C
ENST00000370300.8:c.1373G>C	ENSP00000359323.4:p.Ser458Thr
ENST00000370305.5:c.1151G>C	ENSP00000359328.1:p.Ser384Thr
ENST00000370308.8:n.1479G>C
ENST00000415228.5:c.*429G>C	ENSP00000416397.1:n.*429G>C
ENST00000415954.6:c.1418G>C	ENSP00000402038.2:p.Ser473Thr
ENST00000445187.5:c.412G>C	ENSP00000407580.1:n.412G>C
ENST00000462039.5:n.1320G>C
ENST00000498286.5:c.1298G>C	ENSP00000419561.1:p.Ser433Thr
ENST00000524046.1:c.204-372G>C
NM_001123226.1:c.1418G>C	NP_001116698.1:p.Ser473Thr
NM_012123.3:c.1298G>C	NP_036255.2:p.Ser433Thr
NM_133645.2:c.1373G>C	NP_598400.1:p.Ser458Thr
XM_006715444.2:c.1076G>C	XP_006715507.1:p.Ser359Thr
XM_006715445.2:c.1076G>C	XP_006715508.1:p.Ser359Thr
XM_006715446.2:c.1298G>C	XP_006715509.1:p.Ser433Thr
XM_006715447.2:c.*31G>C	XP_006715510.1:n.*31G>C
XM_011535723.1:c.887G>C	XP_011534025.1:p.Ser296Thr
XM_011535724.1:c.887G>C	XP_011534026.1:p.Ser296Thr
XM_011535725.1:c.887G>C	XP_011534027.1:p.Ser296Thr
NM_001123226.2:c.1418G>C	NP_001116698.1:p.Ser473Thr
NM_012123.4:c.1298G>C MANE Select	NP_036255.2:p.Ser433Thr
NM_133645.3:c.1373G>C	NP_598400.1:p.Ser458Thr