Canonical Allele Identifier: CA2838460493
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331830del , CM000663.2:g.45331830del GRCh38
NC_000001.10:g.45797502del , CM000663.1:g.45797502del GRCh37
NC_000001.9:g.45570089del NCBI36
NG_008189.1:g.13642del , LRG_220:g.13642del

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.550del ENSP00000410263.2:p.His184ThrfsTer?
ENST00000435155.2:c.967del ENSP00000403655.2:p.His323ThrfsTer?
ENST00000467459.6:c.957del ENSP00000435889.2:p.Thr320ProfsTer?
ENST00000483127.2:c.952del ENSP00000436469.2:p.His318ThrfsTer?
ENST00000485271.6:c.934del ENSP00000431264.2:p.His312ThrfsTer?
ENST00000529892.6:c.955+194del ENSP00000432528.2:n.955+194del
ENST00000533178.6:c.*263del ENSP00000436430.2:n.*263del
ENST00000672314.2:c.934del ENSP00000500828.2:p.His312ThrfsTer?
ENST00000710952.2:c.1018del MANE Plus Clinical ENSP00000518552.2:p.His340ThrfsTer?
ENST00000672818.3:c.1009del ENSP00000500891.1:p.His337ThrfsTer?
ENST00000456914.7:c.934del MANE Select ENSP00000407590.2:p.His312ThrfsTer?
ENST00000671898.1:c.1522del ENSP00000499896.1:p.His508ThrfsTer?
ENST00000672011.1:c.*263del ENSP00000500418.1:n.*263del
ENST00000672314.1:c.934del ENSP00000500828.1:p.His312ThrfsTer?
ENST00000672593.1:c.*1160del ENSP00000500455.1:n.*1160del
ENST00000672764.1:c.*263del ENSP00000500886.1:n.*263del
ENST00000672818.2:c.1009del ENSP00000500891.1:p.His337ThrfsTer?
ENST00000673134.1:c.*631del ENSP00000500526.1:n.*631del
ENST00000354383.10:c.937del ENSP00000346354.6:p.His313ThrfsTer?
ENST00000355498.6:c.934del ENSP00000347685.2:p.His312ThrfsTer?
ENST00000372098.7:c.1009del ENSP00000361170.3:p.His337ThrfsTer?
ENST00000372104.5:c.934del ENSP00000361176.1:p.His312ThrfsTer?
ENST00000372110.7:c.979del ENSP00000361182.3:p.His327ThrfsTer?
ENST00000372115.7:c.976del ENSP00000361187.3:p.His326ThrfsTer?
ENST00000412971.5:c.550del ENSP00000410263.1:p.His184ThrfsTer?
ENST00000448481.5:c.967del ENSP00000409718.1:p.His323ThrfsTer?
ENST00000450313.5:c.1018del ENSP00000408176.1:p.His340ThrfsTer?
ENST00000456914.6:c.934del ENSP00000407590.2:p.His312ThrfsTer?
ENST00000462388.5:n.798del
ENST00000466231.1:n.299del
ENST00000467459.5:c.351del ENSP00000435889.1:p.Thr118ProfsTer?
ENST00000475516.5:c.*747del ENSP00000433843.1:n.*747del
ENST00000481571.5:c.*747del ENSP00000436597.1:n.*747del
ENST00000482094.5:n.255del
ENST00000488731.6:c.188-273del ENSP00000432330.1:n.188-273del
ENST00000528013.6:c.976del ENSP00000433130.2:p.His326ThrfsTer?
ENST00000529892.5:c.177+194del
ENST00000529984.5:c.188-273del ENSP00000437093.1:n.188-273del
ENST00000531105.5:c.116-2392del ENSP00000431292.1:n.116-2392del
ENST00000533178.5:c.563del ENSP00000436430.1:n.563del
NM_001048171.1:c.976del NP_001041636.1:p.His326ThrfsTer?
NM_001048172.1:c.937del NP_001041637.1:p.His313ThrfsTer?
NM_001048173.1:c.934del NP_001041638.1:p.His312ThrfsTer?
NM_001048174.1:c.934del NP_001041639.1:p.His312ThrfsTer?
NM_001128425.1:c.1018del , LRG_220t1:c.1018del NP_001121897.1:p.His340ThrfsTer?
NM_001293190.1:c.979del NP_001280119.1:p.His327ThrfsTer?
NM_001293191.1:c.967del NP_001280120.1:p.His323ThrfsTer?
NM_001293192.1:c.658del NP_001280121.1:p.His220ThrfsTer?
NM_001293195.1:c.934del NP_001280124.1:p.His312ThrfsTer?
NM_001293196.1:c.658del NP_001280125.1:p.His220ThrfsTer?
NM_012222.2:c.1009del NP_036354.1:p.His337ThrfsTer?
XM_011541497.1:c.994del XP_011539799.1:p.His332ThrfsTer?
XM_011541498.1:c.976del XP_011539800.1:p.His326ThrfsTer?
XM_011541499.1:c.976del XP_011539801.1:p.His326ThrfsTer?
XM_011541500.1:c.976del XP_011539802.1:p.His326ThrfsTer?
XM_011541501.1:c.976del XP_011539803.1:p.His326ThrfsTer?
XM_011541502.1:c.976del XP_011539804.1:p.His326ThrfsTer?
XM_011541503.1:c.976del XP_011539805.1:p.His326ThrfsTer?
XM_011541504.1:c.967del XP_011539806.1:p.His323ThrfsTer?
XM_011541505.1:c.556del XP_011539807.1:p.His186ThrfsTer?
XM_011541506.1:c.556del XP_011539808.1:p.His186ThrfsTer?
XM_011541507.1:c.547del XP_011539809.1:p.His183ThrfsTer?
XM_011541508.1:c.562del XP_011539810.1:p.His188ThrfsTer?
XR_946658.1:n.1065del
NM_001350650.1:c.589del NP_001337579.1:p.His197ThrfsTer?
NM_001350651.1:c.589del NP_001337580.1:p.His197ThrfsTer?
NR_146882.1:n.1192del
NR_146883.1:n.1006del
XM_011541497.3:c.994del XP_011539799.1:p.His332ThrfsTer?
XM_011541500.3:c.976del XP_011539802.1:p.His326ThrfsTer?
XM_011541501.2:c.976del XP_011539803.1:p.His326ThrfsTer?
XM_011541502.2:c.976del XP_011539804.1:p.His326ThrfsTer?
XM_011541503.2:c.976del XP_011539805.1:p.His326ThrfsTer?
XM_011541504.2:c.967del XP_011539806.1:p.His323ThrfsTer?
XM_011541505.2:c.556del XP_011539807.1:p.His186ThrfsTer?
XM_011541506.2:c.556del XP_011539808.1:p.His186ThrfsTer?
XM_017001331.1:c.976del XP_016856820.1:p.His326ThrfsTer?
XM_017001332.1:c.976del XP_016856821.1:p.His326ThrfsTer?
XM_017001333.1:c.976del XP_016856822.1:p.His326ThrfsTer?
XM_017001334.1:c.937del XP_016856823.1:p.His313ThrfsTer?
XM_017001335.1:c.658del XP_016856824.1:p.His220ThrfsTer?
XM_017001336.1:c.589del XP_016856825.1:p.His197ThrfsTer?
XM_017001337.1:c.589del XP_016856826.1:p.His197ThrfsTer?
XM_024447244.1:c.589del XP_024303012.1:p.His197ThrfsTer?
XM_024447245.1:c.589del XP_024303013.1:p.His197ThrfsTer?
XM_024447248.1:c.547del XP_024303016.1:p.His183ThrfsTer?
XM_024447249.1:c.418del XP_024303017.1:p.His140ThrfsTer?
XM_024447250.1:c.418del XP_024303018.1:p.His140ThrfsTer?
XM_024447251.1:c.418del XP_024303019.1:p.His140ThrfsTer?
XR_001737190.1:n.979del
XR_001737192.1:n.791del
XR_002956643.1:n.971del
XR_002956644.1:n.1506del
XR_946658.2:n.1079del
NM_001048171.2:c.934del NP_001041636.2:p.His312ThrfsTer?
NM_001128425.2:c.1018del MANE Plus Clinical NP_001121897.1:p.His340ThrfsTer?
NM_001048172.2:c.937del NP_001041637.1:p.His313ThrfsTer?
NM_001048173.2:c.934del NP_001041638.1:p.His312ThrfsTer?
NM_001048174.2:c.934del MANE Select NP_001041639.1:p.His312ThrfsTer?
NM_001293190.2:c.979del NP_001280119.1:p.His327ThrfsTer?
NM_001293191.2:c.967del NP_001280120.1:p.His323ThrfsTer?
NM_001293192.2:c.658del NP_001280121.1:p.His220ThrfsTer?
NM_001293195.2:c.934del NP_001280124.1:p.His312ThrfsTer?
NM_001293196.2:c.658del NP_001280125.1:p.His220ThrfsTer?
NM_001350650.2:c.589del NP_001337579.1:p.His197ThrfsTer?
NM_001350651.2:c.589del NP_001337580.1:p.His197ThrfsTer?
NM_012222.3:c.1009del NP_036354.1:p.His337ThrfsTer?
NR_146882.2:n.1162del
NR_146883.2:n.1011del