Canonical Allele Identifier: CA2473710922
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45329403_45329404delinsCT , CM000663.2:g.45329403_45329404delinsCT GRCh38
NC_000001.10:g.45795075_45795076delinsCT , CM000663.1:g.45795075_45795076delinsCT GRCh37
NC_000001.9:g.45567662_45567663delinsCT NCBI36
NG_008189.1:g.16067_16068delinsAG , LRG_220:g.16067_16068delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.1084_1085delinsAG ENSP00000410263.2:p.Ser362=
ENST00000435155.2:c.1501_1502delinsAG ENSP00000403655.2:p.Ser501=
ENST00000467459.6:c.*330_*331delinsAG ENSP00000435889.2:n.*330_*331delinsAG
ENST00000483127.2:c.1486_1487delinsAG ENSP00000436469.2:p.Ser496=
ENST00000485271.6:c.*211_*212delinsAG ENSP00000431264.2:n.*211_*212delinsAG
ENST00000529892.6:c.1321_1322delinsAG ENSP00000432528.2:p.Ser441=
ENST00000533178.6:c.*797_*798delinsAG ENSP00000436430.2:n.*797_*798delinsAG
ENST00000672314.2:c.1468_1469delinsAG ENSP00000500828.2:p.Ser490=
ENST00000710952.2:c.1552_1553delinsAG MANE Plus Clinical ENSP00000518552.2:p.Ser518=
ENST00000672818.3:c.1543_1544delinsAG ENSP00000500891.1:p.Ser515=
ENST00000456914.7:c.1468_1469delinsAG MANE Select ENSP00000407590.2:p.Ser490=
ENST00000671898.1:c.*211_*212delinsAG ENSP00000499896.1:n.*211_*212delinsAG
ENST00000672011.1:c.*797_*798delinsAG ENSP00000500418.1:n.*797_*798delinsAG
ENST00000672818.2:c.1543_1544delinsAG ENSP00000500891.1:p.Ser515=
ENST00000354383.10:c.1471_1472delinsAG ENSP00000346354.6:p.Ser491=
ENST00000355498.6:c.1468_1469delinsAG ENSP00000347685.2:p.Ser490=
ENST00000372098.7:c.1543_1544delinsAG ENSP00000361170.3:p.Ser515=
ENST00000372104.5:c.1468_1469delinsAG ENSP00000361176.1:p.Ser490=
ENST00000372110.7:c.1513_1514delinsAG ENSP00000361182.3:p.Ser505=
ENST00000372115.7:c.1510_1511delinsAG ENSP00000361187.3:p.Ser504=
ENST00000448481.5:c.1501_1502delinsAG ENSP00000409718.1:p.Ser501=
ENST00000450313.5:c.1552_1553delinsAG ENSP00000408176.1:p.Ser518=
ENST00000456914.6:c.1468_1469delinsAG ENSP00000407590.2:p.Ser490=
ENST00000467459.5:c.885_886delinsAG ENSP00000435889.1:n.885_886delinsAG
ENST00000475516.5:c.*1281_*1282delinsAG ENSP00000433843.1:n.*1281_*1282delinsAG
ENST00000481571.5:c.*1281_*1282delinsAG ENSP00000436597.1:n.*1281_*1282delinsAG
ENST00000482094.5:n.789_790delinsAG
ENST00000485271.5:c.345_346delinsAG
ENST00000488731.6:c.553_554delinsAG ENSP00000432330.1:p.Ser185=
ENST00000528013.6:c.1510_1511delinsAG ENSP00000433130.2:p.Ser504=
ENST00000529892.5:c.543_544delinsAG
ENST00000529984.5:c.553_554delinsAG ENSP00000437093.1:p.Ser185=
ENST00000531105.5:c.149_150delinsAG ENSP00000431292.1:p.Gln50=
ENST00000533178.5:c.1097_1098delinsAG ENSP00000436430.1:n.1097_1098delinsAG
NM_001048171.1:c.1510_1511delinsAG NP_001041636.1:p.Ser504=
NM_001048172.1:c.1471_1472delinsAG NP_001041637.1:p.Ser491=
NM_001048173.1:c.1468_1469delinsAG NP_001041638.1:p.Ser490=
NM_001048174.1:c.1468_1469delinsAG NP_001041639.1:p.Ser490=
NM_001128425.1:c.1552_1553delinsAG , LRG_220t1:c.1552_1553delinsAG NP_001121897.1:p.Ser518=
NM_001293190.1:c.1513_1514delinsAG NP_001280119.1:p.Ser505=
NM_001293191.1:c.1501_1502delinsAG NP_001280120.1:p.Ser501=
NM_001293192.1:c.1192_1193delinsAG NP_001280121.1:p.Ser398=
NM_001293195.1:c.1468_1469delinsAG NP_001280124.1:p.Ser490=
NM_001293196.1:c.1192_1193delinsAG NP_001280125.1:p.Ser398=
NM_012222.2:c.1543_1544delinsAG NP_036354.1:p.Ser515=
XM_011541497.1:c.1528_1529delinsAG XP_011539799.1:p.Ser510=
XM_011541498.1:c.1510_1511delinsAG XP_011539800.1:p.Ser504=
XM_011541499.1:c.1510_1511delinsAG XP_011539801.1:p.Ser504=
XM_011541500.1:c.1510_1511delinsAG XP_011539802.1:p.Ser504=
XM_011541501.1:c.1510_1511delinsAG XP_011539803.1:p.Ser504=
XM_011541502.1:c.1510_1511delinsAG XP_011539804.1:p.Ser504=
XM_011541503.1:c.1510_1511delinsAG XP_011539805.1:p.Ser504=
XM_011541504.1:c.1501_1502delinsAG XP_011539806.1:p.Ser501=
XM_011541505.1:c.1090_1091delinsAG XP_011539807.1:p.Ser364=
XM_011541506.1:c.1090_1091delinsAG XP_011539808.1:p.Ser364=
XM_011541507.1:c.1081_1082delinsAG XP_011539809.1:p.Ser361=
XM_011541508.1:c.1096_1097delinsAG XP_011539810.1:p.Ser366=
XR_946658.1:n.1779_1780delinsAG
NM_001350650.1:c.1123_1124delinsAG NP_001337579.1:p.Ser375=
NM_001350651.1:c.1123_1124delinsAG NP_001337580.1:p.Ser375=
NR_146882.1:n.1906_1907delinsAG
NR_146883.1:n.1720_1721delinsAG
XM_011541497.3:c.1528_1529delinsAG XP_011539799.1:p.Ser510=
XM_011541500.3:c.1510_1511delinsAG XP_011539802.1:p.Ser504=
XM_011541501.2:c.1510_1511delinsAG XP_011539803.1:p.Ser504=
XM_011541502.2:c.1510_1511delinsAG XP_011539804.1:p.Ser504=
XM_011541503.2:c.1510_1511delinsAG XP_011539805.1:p.Ser504=
XM_011541504.2:c.1501_1502delinsAG XP_011539806.1:p.Ser501=
XM_011541505.2:c.1090_1091delinsAG XP_011539807.1:p.Ser364=
XM_011541506.2:c.1090_1091delinsAG XP_011539808.1:p.Ser364=
XM_017001331.1:c.1510_1511delinsAG XP_016856820.1:p.Ser504=
XM_017001332.1:c.1510_1511delinsAG XP_016856821.1:p.Ser504=
XM_017001333.1:c.1510_1511delinsAG XP_016856822.1:p.Ser504=
XM_017001334.1:c.1471_1472delinsAG XP_016856823.1:p.Ser491=
XM_017001335.1:c.1192_1193delinsAG XP_016856824.1:p.Ser398=
XM_017001336.1:c.1123_1124delinsAG XP_016856825.1:p.Ser375=
XM_017001337.1:c.1123_1124delinsAG XP_016856826.1:p.Ser375=
XM_024447244.1:c.1123_1124delinsAG XP_024303012.1:p.Ser375=
XM_024447245.1:c.1123_1124delinsAG XP_024303013.1:p.Ser375=
XM_024447248.1:c.1081_1082delinsAG XP_024303016.1:p.Ser361=
XM_024447249.1:c.952_953delinsAG XP_024303017.1:p.Ser318=
XM_024447250.1:c.952_953delinsAG XP_024303018.1:p.Ser318=
XM_024447251.1:c.952_953delinsAG XP_024303019.1:p.Ser318=
XR_001737190.1:n.1693_1694delinsAG
XR_001737192.1:n.1505_1506delinsAG
XR_002956643.1:n.1685_1686delinsAG
XR_002956644.1:n.2220_2221delinsAG
XR_946658.2:n.1793_1794delinsAG
NM_001048171.2:c.1468_1469delinsAG NP_001041636.2:p.Ser490=
NM_001128425.2:c.1552_1553delinsAG MANE Plus Clinical NP_001121897.1:p.Ser518=
NM_001048172.2:c.1471_1472delinsAG NP_001041637.1:p.Ser491=
NM_001048173.2:c.1468_1469delinsAG NP_001041638.1:p.Ser490=
NM_001048174.2:c.1468_1469delinsAG MANE Select NP_001041639.1:p.Ser490=
NM_001293190.2:c.1513_1514delinsAG NP_001280119.1:p.Ser505=
NM_001293191.2:c.1501_1502delinsAG NP_001280120.1:p.Ser501=
NM_001293192.2:c.1192_1193delinsAG NP_001280121.1:p.Ser398=
NM_001293195.2:c.1468_1469delinsAG NP_001280124.1:p.Ser490=
NM_001293196.2:c.1192_1193delinsAG NP_001280125.1:p.Ser398=
NM_001350650.2:c.1123_1124delinsAG NP_001337579.1:p.Ser375=
NM_001350651.2:c.1123_1124delinsAG NP_001337580.1:p.Ser375=
NM_012222.3:c.1543_1544delinsAG NP_036354.1:p.Ser515=
NR_146882.2:n.1876_1877delinsAG
NR_146883.2:n.1725_1726delinsAG