Canonical Allele Identifier: CA16610207
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 406847
ClinVar RCV Id: RCV000460168
dbSNP Id: rs1060501336

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45334447del , CM000663.2:g.45334447del GRCh38
NC_000001.10:g.45800119del , CM000663.1:g.45800119del GRCh37
NC_000001.9:g.45572706del NCBI36
NG_008189.1:g.11025del , LRG_220:g.11025del

Transcript Alleles

HGVS Amino-acid change
ENST00000450313.6:c.102del ENSP00000408176.2:p.Arg36GlyfsTer22
ENST00000456914.7:c.60del MANE Select ENSP00000407590.2:p.Arg22GlyfsTer?
ENST00000461495.6:c.102del ENSP00000437166.1:p.Arg36GlyfsTer21
ENST00000671856.1:n.80del
ENST00000671898.1:c.606del ENSP00000499896.1:p.Arg204GlyfsTer22
ENST00000672011.1:c.102del ENSP00000500418.1:p.Arg36GlyfsTer?
ENST00000672314.1:c.60del ENSP00000500828.1:p.Arg22GlyfsTer?
ENST00000672593.1:c.60del ENSP00000500455.1:p.Arg22GlyfsTer21
ENST00000672764.1:c.60del ENSP00000500886.1:p.Arg22GlyfsTer19
ENST00000672818.2:c.102del ENSP00000500891.1:p.Arg36GlyfsTer19
ENST00000673134.1:c.60del ENSP00000500526.1:p.Arg22GlyfsTer21
ENST00000674679.1:n.32del ENSP00000501623.1:p.Lys11ArgfsTer7
ENST00000354383.10:c.60del ENSP00000346354.6:p.Arg22GlyfsTer?
ENST00000355498.6:c.60del ENSP00000347685.2:p.Arg22GlyfsTer?
ENST00000372098.7:c.102del ENSP00000361170.3:p.Arg36GlyfsTer19
ENST00000372104.5:c.60del ENSP00000361176.1:p.Arg22GlyfsTer?
ENST00000372110.7:c.102del ENSP00000361182.3:p.Arg36GlyfsTer?
ENST00000372115.7:c.102del ENSP00000361187.3:p.Arg36GlyfsTer?
ENST00000412971.5:c.37-1612del ENSP00000410263.1:p.=
ENST00000435155.1:c.60del ENSP00000403655.1:p.Arg22GlyfsTer19
ENST00000448481.5:c.60del ENSP00000409718.1:p.Arg22GlyfsTer19
ENST00000450313.5:c.102del ENSP00000408176.1:p.Arg36GlyfsTer22
ENST00000456914.6:c.60del ENSP00000407590.2:p.Arg22GlyfsTer?
ENST00000461495.5:c.102del ENSP00000437166.1:p.Arg36GlyfsTer21
ENST00000462387.5:n.280del
ENST00000467940.5:c.118del ENSP00000436478.1:p.Arg40GlyfsTer?
ENST00000470256.5:c.60del ENSP00000434985.1:p.Arg22GlyfsTer?
ENST00000474703.1:n.182del
ENST00000475516.5:c.60del ENSP00000433843.1:p.Arg22GlyfsTer21
ENST00000476789.5:n.280del
ENST00000479746.6:n.123del
ENST00000481139.5:n.263del
ENST00000481571.5:c.102del ENSP00000436597.1:p.Arg36GlyfsTer21
ENST00000483127.1:c.78del ENSP00000436469.1:p.Arg28GlyfsTer?
ENST00000483642.5:n.241del
ENST00000485484.5:n.110del
ENST00000488731.6:c.60del ENSP00000432330.1:p.Arg22GlyfsTer?
ENST00000492494.5:n.123del
ENST00000525160.5:c.102del ENSP00000431568.1:p.Arg36GlyfsTer?
ENST00000528013.6:c.60del ENSP00000433130.2:p.Arg22GlyfsTer22
ENST00000529984.5:c.60del ENSP00000437093.1:p.Arg22GlyfsTer?
ENST00000531105.5:c.60del ENSP00000431292.1:p.Arg22GlyfsTer?
ENST00000533178.5:n.66del ENSP00000436430.1:p.Arg24GlyfsTer?
ENST00000534453.1:n.326del
NM_001048171.1:c.102del NP_001041636.1:p.Arg36GlyfsTer?
NM_001048172.1:c.60del NP_001041637.1:p.Arg22GlyfsTer?
NM_001048173.1:c.60del NP_001041638.1:p.Arg22GlyfsTer?
NM_001048174.1:c.60del NP_001041639.1:p.Arg22GlyfsTer?
NM_001128425.1:c.102del , LRG_220t1:c.102del NP_001121897.1:p.Arg36GlyfsTer22
NM_001293190.1:c.102del NP_001280119.1:p.Arg36GlyfsTer?
NM_001293191.1:c.60del NP_001280120.1:p.Arg22GlyfsTer19
NM_001293192.1:c.-153del NP_001280121.1:p.=
NM_001293195.1:c.60del NP_001280124.1:p.Arg22GlyfsTer?
NM_001293196.1:c.-153del NP_001280125.1:p.=
NM_012222.2:c.102del NP_036354.1:p.Arg36GlyfsTer19
XM_011541497.1:c.78del XP_011539799.1:p.Arg28GlyfsTer22
XM_011541498.1:c.60del XP_011539800.1:p.Arg22GlyfsTer22
XM_011541499.1:c.60del XP_011539801.1:p.Arg22GlyfsTer22
XM_011541500.1:c.60del XP_011539802.1:p.Arg22GlyfsTer22
XM_011541501.1:c.60del XP_011539803.1:p.Arg22GlyfsTer22
XM_011541502.1:c.60del XP_011539804.1:p.Arg22GlyfsTer22
XM_011541503.1:c.102del XP_011539805.1:p.Arg36GlyfsTer22
XM_011541504.1:c.60del XP_011539806.1:p.Arg22GlyfsTer19
XM_011541505.1:c.-14del XP_011539807.1:p.=
XM_011541506.1:c.-14del XP_011539808.1:p.=
XR_946658.1:n.149del
NM_001350650.1:c.-212del NP_001337579.1:p.=
NM_001350651.1:c.-148del NP_001337580.1:p.=
NR_146882.1:n.318del
NR_146883.1:n.206del
XM_011541497.3:c.78del XP_011539799.1:p.Arg28GlyfsTer22
XM_011541500.3:c.60del XP_011539802.1:p.Arg22GlyfsTer22
XM_011541501.2:c.60del XP_011539803.1:p.Arg22GlyfsTer22
XM_011541502.2:c.60del XP_011539804.1:p.Arg22GlyfsTer22
XM_011541503.2:c.102del XP_011539805.1:p.Arg36GlyfsTer22
XM_011541504.2:c.60del XP_011539806.1:p.Arg22GlyfsTer19
XM_011541505.2:c.-14del XP_011539807.1:p.=
XM_011541506.2:c.-14del XP_011539808.1:p.=
XM_017001331.1:c.60del XP_016856820.1:p.Arg22GlyfsTer22
XM_017001332.1:c.60del XP_016856821.1:p.Arg22GlyfsTer22
XM_017001333.1:c.60del XP_016856822.1:p.Arg22GlyfsTer22
XM_017001334.1:c.60del XP_016856823.1:p.Arg22GlyfsTer?
XM_017001335.1:c.-153del XP_016856824.1:p.=
XM_017001336.1:c.-245del XP_016856825.1:p.=
XM_017001337.1:c.-245del XP_016856826.1:p.=
XM_024447244.1:c.-254del XP_024303012.1:p.=
XM_024447245.1:c.-215del XP_024303013.1:p.=
XM_024447248.1:c.-212del XP_024303016.1:p.=
XM_024447249.1:c.-708del XP_024303017.1:p.=
XM_024447250.1:c.-711del XP_024303018.1:p.=
XM_024447251.1:c.-402del XP_024303019.1:p.=
XR_001737190.1:n.169del
XR_001737192.1:n.97del
XR_002956643.1:n.277del
XR_002956644.1:n.295del
XR_946658.2:n.163del
NM_001048171.2:c.60del NP_001041636.2:p.Arg22GlyfsTer?
NM_001128425.2:c.102del NP_001121897.1:p.Arg36GlyfsTer22
NM_001048172.2:c.60del NP_001041637.1:p.Arg22GlyfsTer?
NM_001048173.2:c.60del NP_001041638.1:p.Arg22GlyfsTer?
NM_001048174.2:c.60del MANE Select NP_001041639.1:p.Arg22GlyfsTer?
NM_001293190.2:c.102del NP_001280119.1:p.Arg36GlyfsTer?
NM_001293191.2:c.60del NP_001280120.1:p.Arg22GlyfsTer19
NM_001293192.2:c.-153del NP_001280121.1:p.=
NM_001293195.2:c.60del NP_001280124.1:p.Arg22GlyfsTer?
NM_001293196.2:c.-153del NP_001280125.1:p.=
NM_001350650.2:c.-212del NP_001337579.1:p.=
NM_001350651.2:c.-148del NP_001337580.1:p.=
NM_012222.3:c.102del NP_036354.1:p.Arg36GlyfsTer19
NR_146882.2:n.288del
NR_146883.2:n.211del