Canonical Allele Identifier: CA2843004588
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332533dup , CM000663.2:g.45332533dup GRCh38
NC_000001.10:g.45798205dup , CM000663.1:g.45798205dup GRCh37
NC_000001.9:g.45570792dup NCBI36
NG_008189.1:g.12938dup , LRG_220:g.12938dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.222+41dup ENSP00000410263.2:n.222+41dup
ENST00000435155.2:c.639+41dup ENSP00000403655.2:n.639+41dup
ENST00000467459.6:c.606+41dup ENSP00000435889.2:n.606+41dup
ENST00000483127.2:c.624+41dup ENSP00000436469.2:n.624+41dup
ENST00000485271.6:c.606+41dup ENSP00000431264.2:n.606+41dup
ENST00000529892.6:c.648+41dup ENSP00000432528.2:n.648+41dup
ENST00000533178.6:c.229+41dup ENSP00000436430.2:n.229+41dup
ENST00000672314.2:c.606+41dup ENSP00000500828.2:n.606+41dup
ENST00000674679.2:c.*518+41dup ENSP00000501623.2:n.*518+41dup
ENST00000710952.2:c.690+41dup MANE Plus Clinical ENSP00000518552.2:n.690+41dup
ENST00000672818.3:c.681+41dup ENSP00000500891.1:n.681+41dup
ENST00000450313.6:c.616+41dup ENSP00000408176.2:n.616+41dup
ENST00000456914.7:c.606+41dup MANE Select ENSP00000407590.2:n.606+41dup
ENST00000461495.6:c.*345+41dup ENSP00000437166.1:n.*345+41dup
ENST00000671898.1:c.1194+41dup ENSP00000499896.1:n.1194+41dup
ENST00000672011.1:c.574+41dup ENSP00000500418.1:n.574+41dup
ENST00000672314.1:c.606+41dup ENSP00000500828.1:n.606+41dup
ENST00000672593.1:c.*535dup ENSP00000500455.1:n.*535dup
ENST00000672764.1:c.565+41dup ENSP00000500886.1:n.565+41dup
ENST00000672818.2:c.681+41dup ENSP00000500891.1:n.681+41dup
ENST00000673134.1:c.*303+41dup ENSP00000500526.1:n.*303+41dup
ENST00000674679.1:c.634+41dup ENSP00000501623.1:n.634+41dup
ENST00000354383.10:c.609+41dup ENSP00000346354.6:n.609+41dup
ENST00000355498.6:c.606+41dup ENSP00000347685.2:n.606+41dup
ENST00000372098.7:c.681+41dup ENSP00000361170.3:n.681+41dup
ENST00000372104.5:c.606+41dup ENSP00000361176.1:n.606+41dup
ENST00000372110.7:c.651+41dup ENSP00000361182.3:n.651+41dup
ENST00000372115.7:c.648+41dup ENSP00000361187.3:n.648+41dup
ENST00000412971.5:c.222+41dup ENSP00000410263.1:n.222+41dup
ENST00000435155.1:c.639+41dup ENSP00000403655.1:n.639+41dup
ENST00000448481.5:c.639+41dup ENSP00000409718.1:n.639+41dup
ENST00000450313.5:c.690+41dup ENSP00000408176.1:n.690+41dup
ENST00000456914.6:c.606+41dup ENSP00000407590.2:n.606+41dup
ENST00000461495.5:c.*345+41dup ENSP00000437166.1:n.*345+41dup
ENST00000462388.5:n.297+41dup
ENST00000467940.5:c.*529+41dup ENSP00000436478.1:n.*529+41dup
ENST00000470256.5:c.493+41dup ENSP00000434985.1:n.493+41dup
ENST00000475516.5:c.*419+41dup ENSP00000433843.1:n.*419+41dup
ENST00000478796.5:n.593+41dup
ENST00000481571.5:c.*419+41dup ENSP00000436597.1:n.*419+41dup
ENST00000488731.6:c.187+230dup ENSP00000432330.1:n.187+230dup
ENST00000525160.5:c.*257+41dup ENSP00000431568.1:n.*257+41dup
ENST00000528013.6:c.648+41dup ENSP00000433130.2:n.648+41dup
ENST00000529984.5:c.187+230dup ENSP00000437093.1:n.187+230dup
ENST00000531105.5:c.115+1858dup ENSP00000431292.1:n.115+1858dup
ENST00000533178.5:c.235+41dup ENSP00000436430.1:n.235+41dup
NM_001048171.1:c.648+41dup NP_001041636.1:n.648+41dup
NM_001048172.1:c.609+41dup NP_001041637.1:n.609+41dup
NM_001048173.1:c.606+41dup NP_001041638.1:n.606+41dup
NM_001048174.1:c.606+41dup NP_001041639.1:n.606+41dup
NM_001128425.1:c.690+41dup , LRG_220t1:c.690+41dup NP_001121897.1:n.690+41dup
NM_001293190.1:c.651+41dup NP_001280119.1:n.651+41dup
NM_001293191.1:c.639+41dup NP_001280120.1:n.639+41dup
NM_001293192.1:c.330+41dup NP_001280121.1:n.330+41dup
NM_001293195.1:c.606+41dup NP_001280124.1:n.606+41dup
NM_001293196.1:c.330+41dup NP_001280125.1:n.330+41dup
NM_012222.2:c.681+41dup NP_036354.1:n.681+41dup
XM_011541497.1:c.666+41dup XP_011539799.1:n.666+41dup
XM_011541498.1:c.648+41dup XP_011539800.1:n.648+41dup
XM_011541499.1:c.648+41dup XP_011539801.1:n.648+41dup
XM_011541500.1:c.648+41dup XP_011539802.1:n.648+41dup
XM_011541501.1:c.648+41dup XP_011539803.1:n.648+41dup
XM_011541502.1:c.648+41dup XP_011539804.1:n.648+41dup
XM_011541503.1:c.648+41dup XP_011539805.1:n.648+41dup
XM_011541504.1:c.639+41dup XP_011539806.1:n.639+41dup
XM_011541505.1:c.228+41dup XP_011539807.1:n.228+41dup
XM_011541506.1:c.228+41dup XP_011539808.1:n.228+41dup
XM_011541507.1:c.219+41dup XP_011539809.1:n.219+41dup
XM_011541508.1:c.234+41dup XP_011539810.1:n.234+41dup
XR_946658.1:n.737+41dup
NM_001350650.1:c.261+41dup NP_001337579.1:n.261+41dup
NM_001350651.1:c.261+41dup NP_001337580.1:n.261+41dup
NR_146882.1:n.864+41dup
NR_146883.1:n.678+41dup
XM_011541497.3:c.666+41dup XP_011539799.1:n.666+41dup
XM_011541500.3:c.648+41dup XP_011539802.1:n.648+41dup
XM_011541501.2:c.648+41dup XP_011539803.1:n.648+41dup
XM_011541502.2:c.648+41dup XP_011539804.1:n.648+41dup
XM_011541503.2:c.648+41dup XP_011539805.1:n.648+41dup
XM_011541504.2:c.639+41dup XP_011539806.1:n.639+41dup
XM_011541505.2:c.228+41dup XP_011539807.1:n.228+41dup
XM_011541506.2:c.228+41dup XP_011539808.1:n.228+41dup
XM_017001331.1:c.648+41dup XP_016856820.1:n.648+41dup
XM_017001332.1:c.648+41dup XP_016856821.1:n.648+41dup
XM_017001333.1:c.648+41dup XP_016856822.1:n.648+41dup
XM_017001334.1:c.609+41dup XP_016856823.1:n.609+41dup
XM_017001335.1:c.330+41dup XP_016856824.1:n.330+41dup
XM_017001336.1:c.261+41dup XP_016856825.1:n.261+41dup
XM_017001337.1:c.261+41dup XP_016856826.1:n.261+41dup
XM_024447244.1:c.261+41dup XP_024303012.1:n.261+41dup
XM_024447245.1:c.261+41dup XP_024303013.1:n.261+41dup
XM_024447248.1:c.219+41dup XP_024303016.1:n.219+41dup
XM_024447249.1:c.90+41dup XP_024303017.1:n.90+41dup
XM_024447250.1:c.90+41dup XP_024303018.1:n.90+41dup
XM_024447251.1:c.90+41dup XP_024303019.1:n.90+41dup
XR_001737190.1:n.651+41dup
XR_001737192.1:n.463+41dup
XR_002956643.1:n.643+41dup
XR_002956644.1:n.1178+41dup
XR_946658.2:n.751+41dup
NM_001048171.2:c.606+41dup NP_001041636.2:n.606+41dup
NM_001128425.2:c.690+41dup MANE Plus Clinical NP_001121897.1:n.690+41dup
NM_001048172.2:c.609+41dup NP_001041637.1:n.609+41dup
NM_001048173.2:c.606+41dup NP_001041638.1:n.606+41dup
NM_001048174.2:c.606+41dup MANE Select NP_001041639.1:n.606+41dup
NM_001293190.2:c.651+41dup NP_001280119.1:n.651+41dup
NM_001293191.2:c.639+41dup NP_001280120.1:n.639+41dup
NM_001293192.2:c.330+41dup NP_001280121.1:n.330+41dup
NM_001293195.2:c.606+41dup NP_001280124.1:n.606+41dup
NM_001293196.2:c.330+41dup NP_001280125.1:n.330+41dup
NM_001350650.2:c.261+41dup NP_001337579.1:n.261+41dup
NM_001350651.2:c.261+41dup NP_001337580.1:n.261+41dup
NM_012222.3:c.681+41dup NP_036354.1:n.681+41dup
NR_146882.2:n.834+41dup
NR_146883.2:n.683+41dup