Canonical Allele Identifier: CA014723
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 186378
dbSNP Id: rs786202903
gnomAD v2: 1-45800125-C-A
gnomAD v4: 1-45334453-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45334453C>A , CM000663.2:g.45334453C>A GRCh38
NC_000001.10:g.45800125C>A , CM000663.1:g.45800125C>A GRCh37
NC_000001.9:g.45572712C>A NCBI36
NG_008189.1:g.11018G>T , LRG_220:g.11018G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.37-1619G>T ENSP00000410263.2:n.37-1619G>T
ENST00000435155.2:c.53G>T ENSP00000403655.2:p.Ser18Ile
ENST00000467459.6:c.53G>T ENSP00000435889.2:p.Ser18Ile
ENST00000483127.2:c.71G>T ENSP00000436469.2:p.Ser24Ile
ENST00000485271.6:c.53G>T ENSP00000431264.2:p.Ser18Ile
ENST00000529892.6:c.95G>T ENSP00000432528.2:p.Ser32Ile
ENST00000533178.6:c.53G>T ENSP00000436430.2:p.Ser18Ile
ENST00000672314.2:c.53G>T ENSP00000500828.2:p.Ser18Ile
ENST00000674679.2:c.53G>T ENSP00000501623.2:p.Ser18Ile
ENST00000710952.2:c.95G>T MANE Plus Clinical ENSP00000518552.2:p.Ser32Ile
ENST00000672818.3:c.95G>T ENSP00000500891.1:p.Ser32Ile
ENST00000450313.6:c.95G>T ENSP00000408176.2:p.Ser32Ile
ENST00000456914.7:c.53G>T MANE Select ENSP00000407590.2:p.Ser18Ile
ENST00000461495.6:c.95G>T ENSP00000437166.1:p.Ser32Ile
ENST00000671856.1:n.73G>T
ENST00000671898.1:c.599G>T ENSP00000499896.1:p.Ser200Ile
ENST00000672011.1:c.95G>T ENSP00000500418.1:p.Ser32Ile
ENST00000672314.1:c.53G>T ENSP00000500828.1:p.Ser18Ile
ENST00000672593.1:c.53G>T ENSP00000500455.1:p.Ser18Ile
ENST00000672764.1:c.53G>T ENSP00000500886.1:p.Ser18Ile
ENST00000672818.2:c.95G>T ENSP00000500891.1:p.Ser32Ile
ENST00000673134.1:c.53G>T ENSP00000500526.1:p.Ser18Ile
ENST00000674679.1:c.25G>T ENSP00000501623.1:p.Ala9Ser
ENST00000354383.10:c.53G>T ENSP00000346354.6:p.Ser18Ile
ENST00000355498.6:c.53G>T ENSP00000347685.2:p.Ser18Ile
ENST00000372098.7:c.95G>T ENSP00000361170.3:p.Ser32Ile
ENST00000372104.5:c.53G>T ENSP00000361176.1:p.Ser18Ile
ENST00000372110.7:c.95G>T ENSP00000361182.3:p.Ser32Ile
ENST00000372115.7:c.95G>T ENSP00000361187.3:p.Ser32Ile
ENST00000412971.5:c.37-1619G>T ENSP00000410263.1:n.37-1619G>T
ENST00000435155.1:c.53G>T ENSP00000403655.1:p.Ser18Ile
ENST00000448481.5:c.53G>T ENSP00000409718.1:p.Ser18Ile
ENST00000450313.5:c.95G>T ENSP00000408176.1:p.Ser32Ile
ENST00000456914.6:c.53G>T ENSP00000407590.2:p.Ser18Ile
ENST00000461495.5:c.95G>T ENSP00000437166.1:p.Ser32Ile
ENST00000462387.5:n.273G>T
ENST00000467940.5:c.111G>T ENSP00000436478.1:p.Gln37His
ENST00000470256.5:c.53G>T ENSP00000434985.1:p.Ser18Ile
ENST00000474703.1:n.175G>T
ENST00000475516.5:c.53G>T ENSP00000433843.1:p.Ser18Ile
ENST00000476789.5:n.273G>T
ENST00000479746.6:n.116G>T
ENST00000481139.5:n.256G>T
ENST00000481571.5:c.95G>T ENSP00000436597.1:p.Ser32Ile
ENST00000483127.1:c.71G>T ENSP00000436469.1:p.Ser24Ile
ENST00000483642.5:n.234G>T
ENST00000485484.5:n.103G>T
ENST00000488731.6:c.53G>T ENSP00000432330.1:p.Ser18Ile
ENST00000492494.5:n.116G>T
ENST00000525160.5:c.95G>T ENSP00000431568.1:p.Ser32Ile
ENST00000528013.6:c.53G>T ENSP00000433130.2:p.Ser18Ile
ENST00000529984.5:c.53G>T ENSP00000437093.1:p.Ser18Ile
ENST00000531105.5:c.53G>T ENSP00000431292.1:p.Ser18Ile
ENST00000533178.5:c.59G>T ENSP00000436430.1:p.Ser20Ile
ENST00000534453.1:n.319G>T
NM_001048171.1:c.95G>T NP_001041636.1:p.Ser32Ile
NM_001048172.1:c.53G>T NP_001041637.1:p.Ser18Ile
NM_001048173.1:c.53G>T NP_001041638.1:p.Ser18Ile
NM_001048174.1:c.53G>T NP_001041639.1:p.Ser18Ile
NM_001128425.1:c.95G>T , LRG_220t1:c.95G>T NP_001121897.1:p.Ser32Ile
NM_001293190.1:c.95G>T NP_001280119.1:p.Ser32Ile
NM_001293191.1:c.53G>T NP_001280120.1:p.Ser18Ile
NM_001293192.1:c.-160G>T NP_001280121.1:n.-160G>T
NM_001293195.1:c.53G>T NP_001280124.1:p.Ser18Ile
NM_001293196.1:c.-160G>T NP_001280125.1:n.-160G>T
NM_012222.2:c.95G>T NP_036354.1:p.Ser32Ile
XM_011541497.1:c.71G>T XP_011539799.1:p.Ser24Ile
XM_011541498.1:c.53G>T XP_011539800.1:p.Ser18Ile
XM_011541499.1:c.53G>T XP_011539801.1:p.Ser18Ile
XM_011541500.1:c.53G>T XP_011539802.1:p.Ser18Ile
XM_011541501.1:c.53G>T XP_011539803.1:p.Ser18Ile
XM_011541502.1:c.53G>T XP_011539804.1:p.Ser18Ile
XM_011541503.1:c.95G>T XP_011539805.1:p.Ser32Ile
XM_011541504.1:c.53G>T XP_011539806.1:p.Ser18Ile
XM_011541505.1:c.-21G>T XP_011539807.1:n.-21G>T
XM_011541506.1:c.-21G>T XP_011539808.1:n.-21G>T
XR_946658.1:n.142G>T
NM_001350650.1:c.-219G>T NP_001337579.1:n.-219G>T
NM_001350651.1:c.-155G>T NP_001337580.1:n.-155G>T
NR_146882.1:n.311G>T
NR_146883.1:n.199G>T
XM_011541497.3:c.71G>T XP_011539799.1:p.Ser24Ile
XM_011541500.3:c.53G>T XP_011539802.1:p.Ser18Ile
XM_011541501.2:c.53G>T XP_011539803.1:p.Ser18Ile
XM_011541502.2:c.53G>T XP_011539804.1:p.Ser18Ile
XM_011541503.2:c.95G>T XP_011539805.1:p.Ser32Ile
XM_011541504.2:c.53G>T XP_011539806.1:p.Ser18Ile
XM_011541505.2:c.-21G>T XP_011539807.1:n.-21G>T
XM_011541506.2:c.-21G>T XP_011539808.1:n.-21G>T
XM_017001331.1:c.53G>T XP_016856820.1:p.Ser18Ile
XM_017001332.1:c.53G>T XP_016856821.1:p.Ser18Ile
XM_017001333.1:c.53G>T XP_016856822.1:p.Ser18Ile
XM_017001334.1:c.53G>T XP_016856823.1:p.Ser18Ile
XM_017001335.1:c.-160G>T XP_016856824.1:n.-160G>T
XM_017001336.1:c.-252G>T XP_016856825.1:n.-252G>T
XM_017001337.1:c.-252G>T XP_016856826.1:n.-252G>T
XM_024447244.1:c.-261G>T XP_024303012.1:n.-261G>T
XM_024447245.1:c.-222G>T XP_024303013.1:n.-222G>T
XM_024447248.1:c.-219G>T XP_024303016.1:n.-219G>T
XM_024447249.1:c.-715G>T XP_024303017.1:n.-715G>T
XM_024447250.1:c.-718G>T XP_024303018.1:n.-718G>T
XM_024447251.1:c.-409G>T XP_024303019.1:n.-409G>T
XR_001737190.1:n.162G>T
XR_001737192.1:n.90G>T
XR_002956643.1:n.270G>T
XR_002956644.1:n.288G>T
XR_946658.2:n.156G>T
NM_001048171.2:c.53G>T NP_001041636.2:p.Ser18Ile
NM_001128425.2:c.95G>T MANE Plus Clinical NP_001121897.1:p.Ser32Ile
NM_001048172.2:c.53G>T NP_001041637.1:p.Ser18Ile
NM_001048173.2:c.53G>T NP_001041638.1:p.Ser18Ile
NM_001048174.2:c.53G>T MANE Select NP_001041639.1:p.Ser18Ile
NM_001293190.2:c.95G>T NP_001280119.1:p.Ser32Ile
NM_001293191.2:c.53G>T NP_001280120.1:p.Ser18Ile
NM_001293192.2:c.-160G>T NP_001280121.1:n.-160G>T
NM_001293195.2:c.53G>T NP_001280124.1:p.Ser18Ile
NM_001293196.2:c.-160G>T NP_001280125.1:n.-160G>T
NM_001350650.2:c.-219G>T NP_001337579.1:n.-219G>T
NM_001350651.2:c.-155G>T NP_001337580.1:n.-155G>T
NM_012222.3:c.95G>T NP_036354.1:p.Ser32Ile
NR_146882.2:n.281G>T
NR_146883.2:n.204G>T