Canonical Allele Identifier: CA340132647
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1771791
ClinVar RCV Id: RCV002389268

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331258G>A , CM000663.2:g.45331258G>A GRCh38
NC_000001.10:g.45796930G>A , CM000663.1:g.45796930G>A GRCh37
NC_000001.9:g.45569517G>A NCBI36
NG_008189.1:g.14213C>T , LRG_220:g.14213C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.932C>T ENSP00000410263.2:p.Thr311Ile
ENST00000435155.2:c.1349C>T ENSP00000403655.2:p.Thr450Ile
ENST00000467459.6:c.*178C>T ENSP00000435889.2:n.*178C>T
ENST00000483127.2:c.1334C>T ENSP00000436469.2:p.Thr445Ile
ENST00000485271.6:c.1316C>T ENSP00000431264.2:p.Thr439Ile
ENST00000529892.6:c.1169C>T ENSP00000432528.2:p.Thr390Ile
ENST00000533178.6:c.*645C>T ENSP00000436430.2:n.*645C>T
ENST00000672314.2:c.1316C>T ENSP00000500828.2:p.Thr439Ile
ENST00000710952.2:c.1400C>T MANE Plus Clinical ENSP00000518552.2:p.Thr467Ile
ENST00000672818.3:c.1391C>T ENSP00000500891.1:p.Thr464Ile
ENST00000456914.7:c.1316C>T MANE Select ENSP00000407590.2:p.Thr439Ile
ENST00000671898.1:c.1904C>T ENSP00000499896.1:p.Thr635Ile
ENST00000672011.1:c.*645C>T ENSP00000500418.1:n.*645C>T
ENST00000672314.1:c.1316C>T ENSP00000500828.1:p.Thr439Ile
ENST00000672818.2:c.1391C>T ENSP00000500891.1:p.Thr464Ile
ENST00000673134.1:c.*1013C>T ENSP00000500526.1:n.*1013C>T
ENST00000354383.10:c.1319C>T ENSP00000346354.6:p.Thr440Ile
ENST00000355498.6:c.1316C>T ENSP00000347685.2:p.Thr439Ile
ENST00000372098.7:c.1391C>T ENSP00000361170.3:p.Thr464Ile
ENST00000372104.5:c.1316C>T ENSP00000361176.1:p.Thr439Ile
ENST00000372110.7:c.1361C>T ENSP00000361182.3:p.Thr454Ile
ENST00000372115.7:c.1358C>T ENSP00000361187.3:p.Thr453Ile
ENST00000448481.5:c.1349C>T ENSP00000409718.1:p.Thr450Ile
ENST00000450313.5:c.1400C>T ENSP00000408176.1:p.Thr467Ile
ENST00000456914.6:c.1316C>T ENSP00000407590.2:p.Thr439Ile
ENST00000467459.5:c.733C>T ENSP00000435889.1:n.733C>T
ENST00000475516.5:c.*1129C>T ENSP00000433843.1:n.*1129C>T
ENST00000481571.5:c.*1129C>T ENSP00000436597.1:n.*1129C>T
ENST00000482094.5:n.637C>T
ENST00000485271.5:c.13C>T
ENST00000488731.6:c.401C>T ENSP00000432330.1:p.Thr134Ile
ENST00000528013.6:c.1358C>T ENSP00000433130.2:p.Thr453Ile
ENST00000529892.5:c.391C>T
ENST00000529984.5:c.401C>T ENSP00000437093.1:p.Thr134Ile
ENST00000531105.5:c.116-1821C>T ENSP00000431292.1:n.116-1821C>T
ENST00000533178.5:c.945C>T ENSP00000436430.1:n.945C>T
NM_001048171.1:c.1358C>T NP_001041636.1:p.Thr453Ile
NM_001048172.1:c.1319C>T NP_001041637.1:p.Thr440Ile
NM_001048173.1:c.1316C>T NP_001041638.1:p.Thr439Ile
NM_001048174.1:c.1316C>T NP_001041639.1:p.Thr439Ile
NM_001128425.1:c.1400C>T , LRG_220t1:c.1400C>T NP_001121897.1:p.Thr467Ile
NM_001293190.1:c.1361C>T NP_001280119.1:p.Thr454Ile
NM_001293191.1:c.1349C>T NP_001280120.1:p.Thr450Ile
NM_001293192.1:c.1040C>T NP_001280121.1:p.Thr347Ile
NM_001293195.1:c.1316C>T NP_001280124.1:p.Thr439Ile
NM_001293196.1:c.1040C>T NP_001280125.1:p.Thr347Ile
NM_012222.2:c.1391C>T NP_036354.1:p.Thr464Ile
XM_011541497.1:c.1376C>T XP_011539799.1:p.Thr459Ile
XM_011541498.1:c.1358C>T XP_011539800.1:p.Thr453Ile
XM_011541499.1:c.1358C>T XP_011539801.1:p.Thr453Ile
XM_011541500.1:c.1358C>T XP_011539802.1:p.Thr453Ile
XM_011541501.1:c.1358C>T XP_011539803.1:p.Thr453Ile
XM_011541502.1:c.1358C>T XP_011539804.1:p.Thr453Ile
XM_011541503.1:c.1358C>T XP_011539805.1:p.Thr453Ile
XM_011541504.1:c.1349C>T XP_011539806.1:p.Thr450Ile
XM_011541505.1:c.938C>T XP_011539807.1:p.Thr313Ile
XM_011541506.1:c.938C>T XP_011539808.1:p.Thr313Ile
XM_011541507.1:c.929C>T XP_011539809.1:p.Thr310Ile
XM_011541508.1:c.944C>T XP_011539810.1:p.Thr315Ile
XR_946658.1:n.1447C>T
NM_001350650.1:c.971C>T NP_001337579.1:p.Thr324Ile
NM_001350651.1:c.971C>T NP_001337580.1:p.Thr324Ile
NR_146882.1:n.1574C>T
NR_146883.1:n.1388C>T
XM_011541497.3:c.1376C>T XP_011539799.1:p.Thr459Ile
XM_011541500.3:c.1358C>T XP_011539802.1:p.Thr453Ile
XM_011541501.2:c.1358C>T XP_011539803.1:p.Thr453Ile
XM_011541502.2:c.1358C>T XP_011539804.1:p.Thr453Ile
XM_011541503.2:c.1358C>T XP_011539805.1:p.Thr453Ile
XM_011541504.2:c.1349C>T XP_011539806.1:p.Thr450Ile
XM_011541505.2:c.938C>T XP_011539807.1:p.Thr313Ile
XM_011541506.2:c.938C>T XP_011539808.1:p.Thr313Ile
XM_017001331.1:c.1358C>T XP_016856820.1:p.Thr453Ile
XM_017001332.1:c.1358C>T XP_016856821.1:p.Thr453Ile
XM_017001333.1:c.1358C>T XP_016856822.1:p.Thr453Ile
XM_017001334.1:c.1319C>T XP_016856823.1:p.Thr440Ile
XM_017001335.1:c.1040C>T XP_016856824.1:p.Thr347Ile
XM_017001336.1:c.971C>T XP_016856825.1:p.Thr324Ile
XM_017001337.1:c.971C>T XP_016856826.1:p.Thr324Ile
XM_024447244.1:c.971C>T XP_024303012.1:p.Thr324Ile
XM_024447245.1:c.971C>T XP_024303013.1:p.Thr324Ile
XM_024447248.1:c.929C>T XP_024303016.1:p.Thr310Ile
XM_024447249.1:c.800C>T XP_024303017.1:p.Thr267Ile
XM_024447250.1:c.800C>T XP_024303018.1:p.Thr267Ile
XM_024447251.1:c.800C>T XP_024303019.1:p.Thr267Ile
XR_001737190.1:n.1361C>T
XR_001737192.1:n.1173C>T
XR_002956643.1:n.1353C>T
XR_002956644.1:n.1888C>T
XR_946658.2:n.1461C>T
NM_001048171.2:c.1316C>T NP_001041636.2:p.Thr439Ile
NM_001128425.2:c.1400C>T MANE Plus Clinical NP_001121897.1:p.Thr467Ile
NM_001048172.2:c.1319C>T NP_001041637.1:p.Thr440Ile
NM_001048173.2:c.1316C>T NP_001041638.1:p.Thr439Ile
NM_001048174.2:c.1316C>T MANE Select NP_001041639.1:p.Thr439Ile
NM_001293190.2:c.1361C>T NP_001280119.1:p.Thr454Ile
NM_001293191.2:c.1349C>T NP_001280120.1:p.Thr450Ile
NM_001293192.2:c.1040C>T NP_001280121.1:p.Thr347Ile
NM_001293195.2:c.1316C>T NP_001280124.1:p.Thr439Ile
NM_001293196.2:c.1040C>T NP_001280125.1:p.Thr347Ile
NM_001350650.2:c.971C>T NP_001337579.1:p.Thr324Ile
NM_001350651.2:c.971C>T NP_001337580.1:p.Thr324Ile
NM_012222.3:c.1391C>T NP_036354.1:p.Thr464Ile
NR_146882.2:n.1544C>T
NR_146883.2:n.1393C>T