Canonical Allele Identifier: CA012823
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127838
dbSNP Id: rs587778541

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331223_45331225del , CM000663.2:g.45331223_45331225del GRCh38
NC_000001.10:g.45796895_45796897del , CM000663.1:g.45796895_45796897del GRCh37
NC_000001.9:g.45569482_45569484del NCBI36
NG_008189.1:g.14250_14252del , LRG_220:g.14250_14252del

Transcript Alleles

HGVS Amino-acid change
ENST00000456914.7:c.1353_1355del MANE Select ENSP00000407590.2:p.Glu452del
ENST00000671898.1:c.1941_1943del ENSP00000499896.1:p.Glu648del
ENST00000672011.1:c.*682_*684del ENSP00000500418.1:p.=
ENST00000672314.1:c.1353_1355del ENSP00000500828.1:p.Glu452del
ENST00000672818.2:c.1428_1430del ENSP00000500891.1:p.Glu477del
ENST00000673134.1:c.*1050_*1052del ENSP00000500526.1:p.=
ENST00000354383.10:c.1356_1358del ENSP00000346354.6:p.Glu453del
ENST00000355498.6:c.1353_1355del ENSP00000347685.2:p.Glu452del
ENST00000372098.7:c.1428_1430del ENSP00000361170.3:p.Glu477del
ENST00000372104.5:c.1353_1355del ENSP00000361176.1:p.Glu452del
ENST00000372110.7:c.1398_1400del ENSP00000361182.3:p.Glu467del
ENST00000372115.7:c.1395_1397del ENSP00000361187.3:p.Glu466del
ENST00000448481.5:c.1386_1388del ENSP00000409718.1:p.Glu463del
ENST00000450313.5:c.1437_1439del ENSP00000408176.1:p.Glu480del
ENST00000456914.6:c.1353_1355del ENSP00000407590.2:p.Glu452del
ENST00000467459.5:n.770_772del ENSP00000435889.1:p.=
ENST00000475516.5:c.*1166_*1168del ENSP00000433843.1:p.=
ENST00000481571.5:c.*1166_*1168del ENSP00000436597.1:p.=
ENST00000482094.5:n.674_676del
ENST00000485271.5:n.50_52del
ENST00000488731.6:c.438_440del ENSP00000432330.1:p.Glu147del
ENST00000528013.6:c.1395_1397del ENSP00000433130.2:p.Glu466del
ENST00000529892.5:n.428_430del
ENST00000529984.5:c.438_440del ENSP00000437093.1:p.Glu147del
ENST00000531105.5:c.116-1784_116-1782del ENSP00000431292.1:p.=
ENST00000533178.5:n.982_984del ENSP00000436430.1:p.=
NM_001048171.1:c.1395_1397del NP_001041636.1:p.Glu466del
NM_001048172.1:c.1356_1358del NP_001041637.1:p.Glu453del
NM_001048173.1:c.1353_1355del NP_001041638.1:p.Glu452del
NM_001048174.1:c.1353_1355del NP_001041639.1:p.Glu452del
NM_001128425.1:c.1437_1439del , LRG_220t1:c.1437_1439del NP_001121897.1:p.Glu480del
NM_001293190.1:c.1398_1400del NP_001280119.1:p.Glu467del
NM_001293191.1:c.1386_1388del NP_001280120.1:p.Glu463del
NM_001293192.1:c.1077_1079del NP_001280121.1:p.Glu360del
NM_001293195.1:c.1353_1355del NP_001280124.1:p.Glu452del
NM_001293196.1:c.1077_1079del NP_001280125.1:p.Glu360del
NM_012222.2:c.1428_1430del NP_036354.1:p.Glu477del
XM_011541497.1:c.1413_1415del XP_011539799.1:p.Glu472del
XM_011541498.1:c.1395_1397del XP_011539800.1:p.Glu466del
XM_011541499.1:c.1395_1397del XP_011539801.1:p.Glu466del
XM_011541500.1:c.1395_1397del XP_011539802.1:p.Glu466del
XM_011541501.1:c.1395_1397del XP_011539803.1:p.Glu466del
XM_011541502.1:c.1395_1397del XP_011539804.1:p.Glu466del
XM_011541503.1:c.1395_1397del XP_011539805.1:p.Glu466del
XM_011541504.1:c.1386_1388del XP_011539806.1:p.Glu463del
XM_011541505.1:c.975_977del XP_011539807.1:p.Glu326del
XM_011541506.1:c.975_977del XP_011539808.1:p.Glu326del
XM_011541507.1:c.966_968del XP_011539809.1:p.Glu323del
XM_011541508.1:c.981_983del XP_011539810.1:p.Glu328del
XR_946658.1:n.1484_1486del
NM_001350650.1:c.1008_1010del NP_001337579.1:p.Glu337del
NM_001350651.1:c.1008_1010del NP_001337580.1:p.Glu337del
NR_146882.1:n.1611_1613del
NR_146883.1:n.1425_1427del
XM_011541497.3:c.1413_1415del XP_011539799.1:p.Glu472del
XM_011541500.3:c.1395_1397del XP_011539802.1:p.Glu466del
XM_011541501.2:c.1395_1397del XP_011539803.1:p.Glu466del
XM_011541502.2:c.1395_1397del XP_011539804.1:p.Glu466del
XM_011541503.2:c.1395_1397del XP_011539805.1:p.Glu466del
XM_011541504.2:c.1386_1388del XP_011539806.1:p.Glu463del
XM_011541505.2:c.975_977del XP_011539807.1:p.Glu326del
XM_011541506.2:c.975_977del XP_011539808.1:p.Glu326del
XM_017001331.1:c.1395_1397del XP_016856820.1:p.Glu466del
XM_017001332.1:c.1395_1397del XP_016856821.1:p.Glu466del
XM_017001333.1:c.1395_1397del XP_016856822.1:p.Glu466del
XM_017001334.1:c.1356_1358del XP_016856823.1:p.Glu453del
XM_017001335.1:c.1077_1079del XP_016856824.1:p.Glu360del
XM_017001336.1:c.1008_1010del XP_016856825.1:p.Glu337del
XM_017001337.1:c.1008_1010del XP_016856826.1:p.Glu337del
XM_024447244.1:c.1008_1010del XP_024303012.1:p.Glu337del
XM_024447245.1:c.1008_1010del XP_024303013.1:p.Glu337del
XM_024447248.1:c.966_968del XP_024303016.1:p.Glu323del
XM_024447249.1:c.837_839del XP_024303017.1:p.Glu280del
XM_024447250.1:c.837_839del XP_024303018.1:p.Glu280del
XM_024447251.1:c.837_839del XP_024303019.1:p.Glu280del
XR_001737190.1:n.1398_1400del
XR_001737192.1:n.1210_1212del
XR_002956643.1:n.1390_1392del
XR_002956644.1:n.1925_1927del
XR_946658.2:n.1498_1500del
NM_001048171.2:c.1353_1355del NP_001041636.2:p.Glu452del
NM_001128425.2:c.1437_1439del NP_001121897.1:p.Glu480del
NM_001048172.2:c.1356_1358del NP_001041637.1:p.Glu453del
NM_001048173.2:c.1353_1355del NP_001041638.1:p.Glu452del
NM_001048174.2:c.1353_1355del MANE Select NP_001041639.1:p.Glu452del
NM_001293190.2:c.1398_1400del NP_001280119.1:p.Glu467del
NM_001293191.2:c.1386_1388del NP_001280120.1:p.Glu463del
NM_001293192.2:c.1077_1079del NP_001280121.1:p.Glu360del
NM_001293195.2:c.1353_1355del NP_001280124.1:p.Glu452del
NM_001293196.2:c.1077_1079del NP_001280125.1:p.Glu360del
NM_001350650.2:c.1008_1010del NP_001337579.1:p.Glu337del
NM_001350651.2:c.1008_1010del NP_001337580.1:p.Glu337del
NM_012222.3:c.1428_1430del NP_036354.1:p.Glu477del
NR_146882.2:n.1581_1583del
NR_146883.2:n.1430_1432del