Canonical Allele Identifier: CA011618
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41753
dbSNP Id: rs150792276
gnomAD v2: 1-45797139-G-A
gnomAD v3: 1-45331467-G-A
gnomAD v4: 1-45331467-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331467G>A , CM000663.2:g.45331467G>A GRCh38
NC_000001.10:g.45797139G>A , CM000663.1:g.45797139G>A GRCh37
NC_000001.9:g.45569726G>A NCBI36
NG_008189.1:g.14004C>T , LRG_220:g.14004C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.808C>T ENSP00000410263.2:p.Arg270Cys
ENST00000435155.2:c.1225C>T ENSP00000403655.2:p.Arg409Cys
ENST00000467459.6:c.*54C>T ENSP00000435889.2:n.*54C>T
ENST00000483127.2:c.1210C>T ENSP00000436469.2:p.Arg404Cys
ENST00000485271.6:c.1192C>T ENSP00000431264.2:p.Arg398Cys
ENST00000529892.6:c.1045C>T ENSP00000432528.2:p.Arg349Cys
ENST00000533178.6:c.*521C>T ENSP00000436430.2:n.*521C>T
ENST00000672314.2:c.1192C>T ENSP00000500828.2:p.Arg398Cys
ENST00000710952.2:c.1276C>T MANE Plus Clinical ENSP00000518552.2:p.Arg426Cys
ENST00000672818.3:c.1267C>T ENSP00000500891.1:p.Arg423Cys
ENST00000456914.7:c.1192C>T MANE Select ENSP00000407590.2:p.Arg398Cys
ENST00000671898.1:c.1780C>T ENSP00000499896.1:p.Arg594Cys
ENST00000672011.1:c.*521C>T ENSP00000500418.1:n.*521C>T
ENST00000672314.1:c.1192C>T ENSP00000500828.1:p.Arg398Cys
ENST00000672593.1:c.*1418C>T ENSP00000500455.1:n.*1418C>T
ENST00000672818.2:c.1267C>T ENSP00000500891.1:p.Arg423Cys
ENST00000673134.1:c.*889C>T ENSP00000500526.1:n.*889C>T
ENST00000354383.10:c.1195C>T ENSP00000346354.6:p.Arg399Cys
ENST00000355498.6:c.1192C>T ENSP00000347685.2:p.Arg398Cys
ENST00000372098.7:c.1267C>T ENSP00000361170.3:p.Arg423Cys
ENST00000372104.5:c.1192C>T ENSP00000361176.1:p.Arg398Cys
ENST00000372110.7:c.1237C>T ENSP00000361182.3:p.Arg413Cys
ENST00000372115.7:c.1234C>T ENSP00000361187.3:p.Arg412Cys
ENST00000448481.5:c.1225C>T ENSP00000409718.1:p.Arg409Cys
ENST00000450313.5:c.1276C>T ENSP00000408176.1:p.Arg426Cys
ENST00000456914.6:c.1192C>T ENSP00000407590.2:p.Arg398Cys
ENST00000467459.5:c.609C>T ENSP00000435889.1:n.609C>T
ENST00000475516.5:c.*1005C>T ENSP00000433843.1:n.*1005C>T
ENST00000481571.5:c.*1005C>T ENSP00000436597.1:n.*1005C>T
ENST00000482094.5:n.513C>T
ENST00000488731.6:c.277C>T ENSP00000432330.1:p.Arg93Cys
ENST00000528013.6:c.1234C>T ENSP00000433130.2:p.Arg412Cys
ENST00000529892.5:c.267C>T
ENST00000529984.5:c.277C>T ENSP00000437093.1:p.Arg93Cys
ENST00000531105.5:c.116-2030C>T ENSP00000431292.1:n.116-2030C>T
ENST00000533178.5:c.821C>T ENSP00000436430.1:n.821C>T
NM_001048171.1:c.1234C>T NP_001041636.1:p.Arg412Cys
NM_001048172.1:c.1195C>T NP_001041637.1:p.Arg399Cys
NM_001048173.1:c.1192C>T NP_001041638.1:p.Arg398Cys
NM_001048174.1:c.1192C>T NP_001041639.1:p.Arg398Cys
NM_001128425.1:c.1276C>T , LRG_220t1:c.1276C>T NP_001121897.1:p.Arg426Cys
NM_001293190.1:c.1237C>T NP_001280119.1:p.Arg413Cys
NM_001293191.1:c.1225C>T NP_001280120.1:p.Arg409Cys
NM_001293192.1:c.916C>T NP_001280121.1:p.Arg306Cys
NM_001293195.1:c.1192C>T NP_001280124.1:p.Arg398Cys
NM_001293196.1:c.916C>T NP_001280125.1:p.Arg306Cys
NM_012222.2:c.1267C>T NP_036354.1:p.Arg423Cys
XM_011541497.1:c.1252C>T XP_011539799.1:p.Arg418Cys
XM_011541498.1:c.1234C>T XP_011539800.1:p.Arg412Cys
XM_011541499.1:c.1234C>T XP_011539801.1:p.Arg412Cys
XM_011541500.1:c.1234C>T XP_011539802.1:p.Arg412Cys
XM_011541501.1:c.1234C>T XP_011539803.1:p.Arg412Cys
XM_011541502.1:c.1234C>T XP_011539804.1:p.Arg412Cys
XM_011541503.1:c.1234C>T XP_011539805.1:p.Arg412Cys
XM_011541504.1:c.1225C>T XP_011539806.1:p.Arg409Cys
XM_011541505.1:c.814C>T XP_011539807.1:p.Arg272Cys
XM_011541506.1:c.814C>T XP_011539808.1:p.Arg272Cys
XM_011541507.1:c.805C>T XP_011539809.1:p.Arg269Cys
XM_011541508.1:c.820C>T XP_011539810.1:p.Arg274Cys
XR_946658.1:n.1323C>T
NM_001350650.1:c.847C>T NP_001337579.1:p.Arg283Cys
NM_001350651.1:c.847C>T NP_001337580.1:p.Arg283Cys
NR_146882.1:n.1450C>T
NR_146883.1:n.1264C>T
XM_011541497.3:c.1252C>T XP_011539799.1:p.Arg418Cys
XM_011541500.3:c.1234C>T XP_011539802.1:p.Arg412Cys
XM_011541501.2:c.1234C>T XP_011539803.1:p.Arg412Cys
XM_011541502.2:c.1234C>T XP_011539804.1:p.Arg412Cys
XM_011541503.2:c.1234C>T XP_011539805.1:p.Arg412Cys
XM_011541504.2:c.1225C>T XP_011539806.1:p.Arg409Cys
XM_011541505.2:c.814C>T XP_011539807.1:p.Arg272Cys
XM_011541506.2:c.814C>T XP_011539808.1:p.Arg272Cys
XM_017001331.1:c.1234C>T XP_016856820.1:p.Arg412Cys
XM_017001332.1:c.1234C>T XP_016856821.1:p.Arg412Cys
XM_017001333.1:c.1234C>T XP_016856822.1:p.Arg412Cys
XM_017001334.1:c.1195C>T XP_016856823.1:p.Arg399Cys
XM_017001335.1:c.916C>T XP_016856824.1:p.Arg306Cys
XM_017001336.1:c.847C>T XP_016856825.1:p.Arg283Cys
XM_017001337.1:c.847C>T XP_016856826.1:p.Arg283Cys
XM_024447244.1:c.847C>T XP_024303012.1:p.Arg283Cys
XM_024447245.1:c.847C>T XP_024303013.1:p.Arg283Cys
XM_024447248.1:c.805C>T XP_024303016.1:p.Arg269Cys
XM_024447249.1:c.676C>T XP_024303017.1:p.Arg226Cys
XM_024447250.1:c.676C>T XP_024303018.1:p.Arg226Cys
XM_024447251.1:c.676C>T XP_024303019.1:p.Arg226Cys
XR_001737190.1:n.1237C>T
XR_001737192.1:n.1049C>T
XR_002956643.1:n.1229C>T
XR_002956644.1:n.1764C>T
XR_946658.2:n.1337C>T
NM_001048171.2:c.1192C>T NP_001041636.2:p.Arg398Cys
NM_001128425.2:c.1276C>T MANE Plus Clinical NP_001121897.1:p.Arg426Cys
NM_001048172.2:c.1195C>T NP_001041637.1:p.Arg399Cys
NM_001048173.2:c.1192C>T NP_001041638.1:p.Arg398Cys
NM_001048174.2:c.1192C>T MANE Select NP_001041639.1:p.Arg398Cys
NM_001293190.2:c.1237C>T NP_001280119.1:p.Arg413Cys
NM_001293191.2:c.1225C>T NP_001280120.1:p.Arg409Cys
NM_001293192.2:c.916C>T NP_001280121.1:p.Arg306Cys
NM_001293195.2:c.1192C>T NP_001280124.1:p.Arg398Cys
NM_001293196.2:c.916C>T NP_001280125.1:p.Arg306Cys
NM_001350650.2:c.847C>T NP_001337579.1:p.Arg283Cys
NM_001350651.2:c.847C>T NP_001337580.1:p.Arg283Cys
NM_012222.3:c.1267C>T NP_036354.1:p.Arg423Cys
NR_146882.2:n.1420C>T
NR_146883.2:n.1269C>T