Canonical Allele Identifier: CA056342
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 418800
dbSNP Id: rs767747402
gnomAD v2: 1-45796900-G-T
gnomAD v3: 1-45331228-G-T
gnomAD v4: 1-45331228-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331228G>T , CM000663.2:g.45331228G>T GRCh38
NC_000001.10:g.45796900G>T , CM000663.1:g.45796900G>T GRCh37
NC_000001.9:g.45569487G>T NCBI36
NG_008189.1:g.14243C>A , LRG_220:g.14243C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.962C>A ENSP00000410263.2:p.Thr321Lys
ENST00000435155.2:c.1379C>A ENSP00000403655.2:p.Thr460Lys
ENST00000467459.6:c.*208C>A ENSP00000435889.2:n.*208C>A
ENST00000483127.2:c.1364C>A ENSP00000436469.2:p.Thr455Lys
ENST00000485271.6:c.1346C>A ENSP00000431264.2:p.Thr449Lys
ENST00000529892.6:c.1199C>A ENSP00000432528.2:p.Thr400Lys
ENST00000533178.6:c.*675C>A ENSP00000436430.2:n.*675C>A
ENST00000672314.2:c.1346C>A ENSP00000500828.2:p.Thr449Lys
ENST00000710952.2:c.1430C>A MANE Plus Clinical ENSP00000518552.2:p.Thr477Lys
ENST00000672818.3:c.1421C>A ENSP00000500891.1:p.Thr474Lys
ENST00000456914.7:c.1346C>A MANE Select ENSP00000407590.2:p.Thr449Lys
ENST00000671898.1:c.1934C>A ENSP00000499896.1:p.Thr645Lys
ENST00000672011.1:c.*675C>A ENSP00000500418.1:n.*675C>A
ENST00000672314.1:c.1346C>A ENSP00000500828.1:p.Thr449Lys
ENST00000672818.2:c.1421C>A ENSP00000500891.1:p.Thr474Lys
ENST00000673134.1:c.*1043C>A ENSP00000500526.1:n.*1043C>A
ENST00000354383.10:c.1349C>A ENSP00000346354.6:p.Thr450Lys
ENST00000355498.6:c.1346C>A ENSP00000347685.2:p.Thr449Lys
ENST00000372098.7:c.1421C>A ENSP00000361170.3:p.Thr474Lys
ENST00000372104.5:c.1346C>A ENSP00000361176.1:p.Thr449Lys
ENST00000372110.7:c.1391C>A ENSP00000361182.3:p.Thr464Lys
ENST00000372115.7:c.1388C>A ENSP00000361187.3:p.Thr463Lys
ENST00000448481.5:c.1379C>A ENSP00000409718.1:p.Thr460Lys
ENST00000450313.5:c.1430C>A ENSP00000408176.1:p.Thr477Lys
ENST00000456914.6:c.1346C>A ENSP00000407590.2:p.Thr449Lys
ENST00000467459.5:c.763C>A ENSP00000435889.1:n.763C>A
ENST00000475516.5:c.*1159C>A ENSP00000433843.1:n.*1159C>A
ENST00000481571.5:c.*1159C>A ENSP00000436597.1:n.*1159C>A
ENST00000482094.5:n.667C>A
ENST00000485271.5:c.43C>A
ENST00000488731.6:c.431C>A ENSP00000432330.1:p.Thr144Lys
ENST00000528013.6:c.1388C>A ENSP00000433130.2:p.Thr463Lys
ENST00000529892.5:c.421C>A
ENST00000529984.5:c.431C>A ENSP00000437093.1:p.Thr144Lys
ENST00000531105.5:c.116-1791C>A ENSP00000431292.1:n.116-1791C>A
ENST00000533178.5:c.975C>A ENSP00000436430.1:n.975C>A
NM_001048171.1:c.1388C>A NP_001041636.1:p.Thr463Lys
NM_001048172.1:c.1349C>A NP_001041637.1:p.Thr450Lys
NM_001048173.1:c.1346C>A NP_001041638.1:p.Thr449Lys
NM_001048174.1:c.1346C>A NP_001041639.1:p.Thr449Lys
NM_001128425.1:c.1430C>A , LRG_220t1:c.1430C>A NP_001121897.1:p.Thr477Lys
NM_001293190.1:c.1391C>A NP_001280119.1:p.Thr464Lys
NM_001293191.1:c.1379C>A NP_001280120.1:p.Thr460Lys
NM_001293192.1:c.1070C>A NP_001280121.1:p.Thr357Lys
NM_001293195.1:c.1346C>A NP_001280124.1:p.Thr449Lys
NM_001293196.1:c.1070C>A NP_001280125.1:p.Thr357Lys
NM_012222.2:c.1421C>A NP_036354.1:p.Thr474Lys
XM_011541497.1:c.1406C>A XP_011539799.1:p.Thr469Lys
XM_011541498.1:c.1388C>A XP_011539800.1:p.Thr463Lys
XM_011541499.1:c.1388C>A XP_011539801.1:p.Thr463Lys
XM_011541500.1:c.1388C>A XP_011539802.1:p.Thr463Lys
XM_011541501.1:c.1388C>A XP_011539803.1:p.Thr463Lys
XM_011541502.1:c.1388C>A XP_011539804.1:p.Thr463Lys
XM_011541503.1:c.1388C>A XP_011539805.1:p.Thr463Lys
XM_011541504.1:c.1379C>A XP_011539806.1:p.Thr460Lys
XM_011541505.1:c.968C>A XP_011539807.1:p.Thr323Lys
XM_011541506.1:c.968C>A XP_011539808.1:p.Thr323Lys
XM_011541507.1:c.959C>A XP_011539809.1:p.Thr320Lys
XM_011541508.1:c.974C>A XP_011539810.1:p.Thr325Lys
XR_946658.1:n.1477C>A
NM_001350650.1:c.1001C>A NP_001337579.1:p.Thr334Lys
NM_001350651.1:c.1001C>A NP_001337580.1:p.Thr334Lys
NR_146882.1:n.1604C>A
NR_146883.1:n.1418C>A
XM_011541497.3:c.1406C>A XP_011539799.1:p.Thr469Lys
XM_011541500.3:c.1388C>A XP_011539802.1:p.Thr463Lys
XM_011541501.2:c.1388C>A XP_011539803.1:p.Thr463Lys
XM_011541502.2:c.1388C>A XP_011539804.1:p.Thr463Lys
XM_011541503.2:c.1388C>A XP_011539805.1:p.Thr463Lys
XM_011541504.2:c.1379C>A XP_011539806.1:p.Thr460Lys
XM_011541505.2:c.968C>A XP_011539807.1:p.Thr323Lys
XM_011541506.2:c.968C>A XP_011539808.1:p.Thr323Lys
XM_017001331.1:c.1388C>A XP_016856820.1:p.Thr463Lys
XM_017001332.1:c.1388C>A XP_016856821.1:p.Thr463Lys
XM_017001333.1:c.1388C>A XP_016856822.1:p.Thr463Lys
XM_017001334.1:c.1349C>A XP_016856823.1:p.Thr450Lys
XM_017001335.1:c.1070C>A XP_016856824.1:p.Thr357Lys
XM_017001336.1:c.1001C>A XP_016856825.1:p.Thr334Lys
XM_017001337.1:c.1001C>A XP_016856826.1:p.Thr334Lys
XM_024447244.1:c.1001C>A XP_024303012.1:p.Thr334Lys
XM_024447245.1:c.1001C>A XP_024303013.1:p.Thr334Lys
XM_024447248.1:c.959C>A XP_024303016.1:p.Thr320Lys
XM_024447249.1:c.830C>A XP_024303017.1:p.Thr277Lys
XM_024447250.1:c.830C>A XP_024303018.1:p.Thr277Lys
XM_024447251.1:c.830C>A XP_024303019.1:p.Thr277Lys
XR_001737190.1:n.1391C>A
XR_001737192.1:n.1203C>A
XR_002956643.1:n.1383C>A
XR_002956644.1:n.1918C>A
XR_946658.2:n.1491C>A
NM_001048171.2:c.1346C>A NP_001041636.2:p.Thr449Lys
NM_001128425.2:c.1430C>A MANE Plus Clinical NP_001121897.1:p.Thr477Lys
NM_001048172.2:c.1349C>A NP_001041637.1:p.Thr450Lys
NM_001048173.2:c.1346C>A NP_001041638.1:p.Thr449Lys
NM_001048174.2:c.1346C>A MANE Select NP_001041639.1:p.Thr449Lys
NM_001293190.2:c.1391C>A NP_001280119.1:p.Thr464Lys
NM_001293191.2:c.1379C>A NP_001280120.1:p.Thr460Lys
NM_001293192.2:c.1070C>A NP_001280121.1:p.Thr357Lys
NM_001293195.2:c.1346C>A NP_001280124.1:p.Thr449Lys
NM_001293196.2:c.1070C>A NP_001280125.1:p.Thr357Lys
NM_001350650.2:c.1001C>A NP_001337579.1:p.Thr334Lys
NM_001350651.2:c.1001C>A NP_001337580.1:p.Thr334Lys
NM_012222.3:c.1421C>A NP_036354.1:p.Thr474Lys
NR_146882.2:n.1574C>A
NR_146883.2:n.1423C>A