Canonical Allele Identifier: CA340134389
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 629183
ClinVar RCV Id: RCV000773876
dbSNP Id: rs1557470128
gnomAD v3: 1-45332198-G-A
gnomAD v4: 1-45332198-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332198G>A , CM000663.2:g.45332198G>A GRCh38
NC_000001.10:g.45797870G>A , CM000663.1:g.45797870G>A GRCh37
NC_000001.9:g.45570457G>A NCBI36
NG_008189.1:g.13273C>T , LRG_220:g.13273C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.433C>T ENSP00000410263.2:p.Pro145Ser
ENST00000435155.2:c.850C>T ENSP00000403655.2:p.Pro284Ser
ENST00000467459.6:c.817C>T ENSP00000435889.2:p.Pro273Ser
ENST00000483127.2:c.835C>T ENSP00000436469.2:p.Pro279Ser
ENST00000485271.6:c.817C>T ENSP00000431264.2:p.Pro273Ser
ENST00000529892.6:c.859C>T ENSP00000432528.2:p.Pro287Ser
ENST00000533178.6:c.*146C>T ENSP00000436430.2:n.*146C>T
ENST00000672314.2:c.817C>T ENSP00000500828.2:p.Pro273Ser
ENST00000710952.2:c.901C>T MANE Plus Clinical ENSP00000518552.2:p.Pro301Ser
ENST00000672818.3:c.892C>T ENSP00000500891.1:p.Pro298Ser
ENST00000450313.6:c.*146C>T ENSP00000408176.2:n.*146C>T
ENST00000456914.7:c.817C>T MANE Select ENSP00000407590.2:p.Pro273Ser
ENST00000461495.6:c.*556C>T ENSP00000437166.1:n.*556C>T
ENST00000671898.1:c.1405C>T ENSP00000499896.1:p.Pro469Ser
ENST00000672011.1:c.*146C>T ENSP00000500418.1:n.*146C>T
ENST00000672314.1:c.817C>T ENSP00000500828.1:p.Pro273Ser
ENST00000672593.1:c.*870C>T ENSP00000500455.1:n.*870C>T
ENST00000672764.1:c.*146C>T ENSP00000500886.1:n.*146C>T
ENST00000672818.2:c.892C>T ENSP00000500891.1:p.Pro298Ser
ENST00000673134.1:c.*514C>T ENSP00000500526.1:n.*514C>T
ENST00000354383.10:c.820C>T ENSP00000346354.6:p.Pro274Ser
ENST00000355498.6:c.817C>T ENSP00000347685.2:p.Pro273Ser
ENST00000372098.7:c.892C>T ENSP00000361170.3:p.Pro298Ser
ENST00000372104.5:c.817C>T ENSP00000361176.1:p.Pro273Ser
ENST00000372110.7:c.862C>T ENSP00000361182.3:p.Pro288Ser
ENST00000372115.7:c.859C>T ENSP00000361187.3:p.Pro287Ser
ENST00000412971.5:c.433C>T ENSP00000410263.1:p.Pro145Ser
ENST00000435155.1:c.850C>T ENSP00000403655.1:p.Pro284Ser
ENST00000448481.5:c.850C>T ENSP00000409718.1:p.Pro284Ser
ENST00000450313.5:c.901C>T ENSP00000408176.1:p.Pro301Ser
ENST00000456914.6:c.817C>T ENSP00000407590.2:p.Pro273Ser
ENST00000461495.5:c.*556C>T ENSP00000437166.1:n.*556C>T
ENST00000462388.5:n.508C>T
ENST00000466231.1:n.182C>T
ENST00000467459.5:c.211C>T ENSP00000435889.1:p.Pro71Ser
ENST00000470256.5:c.*146C>T ENSP00000434985.1:n.*146C>T
ENST00000475516.5:c.*630C>T ENSP00000433843.1:n.*630C>T
ENST00000481571.5:c.*630C>T ENSP00000436597.1:n.*630C>T
ENST00000488731.6:c.187+565C>T ENSP00000432330.1:n.187+565C>T
ENST00000528013.6:c.859C>T ENSP00000433130.2:p.Pro287Ser
ENST00000529892.5:c.81C>T
ENST00000529984.5:c.187+565C>T ENSP00000437093.1:n.187+565C>T
ENST00000531105.5:c.115+2193C>T ENSP00000431292.1:n.115+2193C>T
ENST00000533178.5:c.446C>T ENSP00000436430.1:n.446C>T
NM_001048171.1:c.859C>T NP_001041636.1:p.Pro287Ser
NM_001048172.1:c.820C>T NP_001041637.1:p.Pro274Ser
NM_001048173.1:c.817C>T NP_001041638.1:p.Pro273Ser
NM_001048174.1:c.817C>T NP_001041639.1:p.Pro273Ser
NM_001128425.1:c.901C>T , LRG_220t1:c.901C>T NP_001121897.1:p.Pro301Ser
NM_001293190.1:c.862C>T NP_001280119.1:p.Pro288Ser
NM_001293191.1:c.850C>T NP_001280120.1:p.Pro284Ser
NM_001293192.1:c.541C>T NP_001280121.1:p.Pro181Ser
NM_001293195.1:c.817C>T NP_001280124.1:p.Pro273Ser
NM_001293196.1:c.541C>T NP_001280125.1:p.Pro181Ser
NM_012222.2:c.892C>T NP_036354.1:p.Pro298Ser
XM_011541497.1:c.877C>T XP_011539799.1:p.Pro293Ser
XM_011541498.1:c.859C>T XP_011539800.1:p.Pro287Ser
XM_011541499.1:c.859C>T XP_011539801.1:p.Pro287Ser
XM_011541500.1:c.859C>T XP_011539802.1:p.Pro287Ser
XM_011541501.1:c.859C>T XP_011539803.1:p.Pro287Ser
XM_011541502.1:c.859C>T XP_011539804.1:p.Pro287Ser
XM_011541503.1:c.859C>T XP_011539805.1:p.Pro287Ser
XM_011541504.1:c.850C>T XP_011539806.1:p.Pro284Ser
XM_011541505.1:c.439C>T XP_011539807.1:p.Pro147Ser
XM_011541506.1:c.439C>T XP_011539808.1:p.Pro147Ser
XM_011541507.1:c.430C>T XP_011539809.1:p.Pro144Ser
XM_011541508.1:c.445C>T XP_011539810.1:p.Pro149Ser
XR_946658.1:n.948C>T
NM_001350650.1:c.472C>T NP_001337579.1:p.Pro158Ser
NM_001350651.1:c.472C>T NP_001337580.1:p.Pro158Ser
NR_146882.1:n.1075C>T
NR_146883.1:n.889C>T
XM_011541497.3:c.877C>T XP_011539799.1:p.Pro293Ser
XM_011541500.3:c.859C>T XP_011539802.1:p.Pro287Ser
XM_011541501.2:c.859C>T XP_011539803.1:p.Pro287Ser
XM_011541502.2:c.859C>T XP_011539804.1:p.Pro287Ser
XM_011541503.2:c.859C>T XP_011539805.1:p.Pro287Ser
XM_011541504.2:c.850C>T XP_011539806.1:p.Pro284Ser
XM_011541505.2:c.439C>T XP_011539807.1:p.Pro147Ser
XM_011541506.2:c.439C>T XP_011539808.1:p.Pro147Ser
XM_017001331.1:c.859C>T XP_016856820.1:p.Pro287Ser
XM_017001332.1:c.859C>T XP_016856821.1:p.Pro287Ser
XM_017001333.1:c.859C>T XP_016856822.1:p.Pro287Ser
XM_017001334.1:c.820C>T XP_016856823.1:p.Pro274Ser
XM_017001335.1:c.541C>T XP_016856824.1:p.Pro181Ser
XM_017001336.1:c.472C>T XP_016856825.1:p.Pro158Ser
XM_017001337.1:c.472C>T XP_016856826.1:p.Pro158Ser
XM_024447244.1:c.472C>T XP_024303012.1:p.Pro158Ser
XM_024447245.1:c.472C>T XP_024303013.1:p.Pro158Ser
XM_024447248.1:c.430C>T XP_024303016.1:p.Pro144Ser
XM_024447249.1:c.301C>T XP_024303017.1:p.Pro101Ser
XM_024447250.1:c.301C>T XP_024303018.1:p.Pro101Ser
XM_024447251.1:c.301C>T XP_024303019.1:p.Pro101Ser
XR_001737190.1:n.862C>T
XR_001737192.1:n.674C>T
XR_002956643.1:n.854C>T
XR_002956644.1:n.1389C>T
XR_946658.2:n.962C>T
NM_001048171.2:c.817C>T NP_001041636.2:p.Pro273Ser
NM_001128425.2:c.901C>T MANE Plus Clinical NP_001121897.1:p.Pro301Ser
NM_001048172.2:c.820C>T NP_001041637.1:p.Pro274Ser
NM_001048173.2:c.817C>T NP_001041638.1:p.Pro273Ser
NM_001048174.2:c.817C>T MANE Select NP_001041639.1:p.Pro273Ser
NM_001293190.2:c.862C>T NP_001280119.1:p.Pro288Ser
NM_001293191.2:c.850C>T NP_001280120.1:p.Pro284Ser
NM_001293192.2:c.541C>T NP_001280121.1:p.Pro181Ser
NM_001293195.2:c.817C>T NP_001280124.1:p.Pro273Ser
NM_001293196.2:c.541C>T NP_001280125.1:p.Pro181Ser
NM_001350650.2:c.472C>T NP_001337579.1:p.Pro158Ser
NM_001350651.2:c.472C>T NP_001337580.1:p.Pro158Ser
NM_012222.3:c.892C>T NP_036354.1:p.Pro298Ser
NR_146882.2:n.1045C>T
NR_146883.2:n.894C>T