Canonical Allele Identifier: CA2695824103
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs569146796
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331984C>A , CM000663.2:g.45331984C>A GRCh38
NC_000001.10:g.45797656C>A , CM000663.1:g.45797656C>A GRCh37
NC_000001.9:g.45570243C>A NCBI36
NG_008189.1:g.13487G>T , LRG_220:g.13487G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.529+39G>T ENSP00000410263.2:n.529+39G>T
ENST00000435155.2:c.946+39G>T ENSP00000403655.2:n.946+39G>T
ENST00000467459.6:c.913+39G>T ENSP00000435889.2:n.913+39G>T
ENST00000483127.2:c.931+39G>T ENSP00000436469.2:n.931+39G>T
ENST00000485271.6:c.913+39G>T ENSP00000431264.2:n.913+39G>T
ENST00000529892.6:c.955+39G>T ENSP00000432528.2:n.955+39G>T
ENST00000533178.6:c.*242+39G>T ENSP00000436430.2:n.*242+39G>T
ENST00000672314.2:c.913+39G>T ENSP00000500828.2:n.913+39G>T
ENST00000710952.2:c.997+39G>T MANE Plus Clinical ENSP00000518552.2:n.997+39G>T
ENST00000672818.3:c.988+39G>T ENSP00000500891.1:n.988+39G>T
ENST00000456914.7:c.913+39G>T MANE Select ENSP00000407590.2:n.913+39G>T
ENST00000671898.1:c.1501+39G>T ENSP00000499896.1:n.1501+39G>T
ENST00000672011.1:c.*242+39G>T ENSP00000500418.1:n.*242+39G>T
ENST00000672314.1:c.913+39G>T ENSP00000500828.1:n.913+39G>T
ENST00000672593.1:c.*1005G>T ENSP00000500455.1:n.*1005G>T
ENST00000672764.1:c.*242+39G>T ENSP00000500886.1:n.*242+39G>T
ENST00000672818.2:c.988+39G>T ENSP00000500891.1:n.988+39G>T
ENST00000673134.1:c.*610+39G>T ENSP00000500526.1:n.*610+39G>T
ENST00000354383.10:c.916+39G>T ENSP00000346354.6:n.916+39G>T
ENST00000355498.6:c.913+39G>T ENSP00000347685.2:n.913+39G>T
ENST00000372098.7:c.988+39G>T ENSP00000361170.3:n.988+39G>T
ENST00000372104.5:c.913+39G>T ENSP00000361176.1:n.913+39G>T
ENST00000372110.7:c.958+39G>T ENSP00000361182.3:n.958+39G>T
ENST00000372115.7:c.955+39G>T ENSP00000361187.3:n.955+39G>T
ENST00000412971.5:c.529+39G>T ENSP00000410263.1:n.529+39G>T
ENST00000448481.5:c.946+39G>T ENSP00000409718.1:n.946+39G>T
ENST00000450313.5:c.997+39G>T ENSP00000408176.1:n.997+39G>T
ENST00000456914.6:c.913+39G>T ENSP00000407590.2:n.913+39G>T
ENST00000462388.5:n.643G>T
ENST00000466231.1:n.278+39G>T
ENST00000467459.5:c.307+39G>T ENSP00000435889.1:n.307+39G>T
ENST00000475516.5:c.*726+39G>T ENSP00000433843.1:n.*726+39G>T
ENST00000481571.5:c.*726+39G>T ENSP00000436597.1:n.*726+39G>T
ENST00000482094.5:n.100G>T
ENST00000488731.6:c.188-428G>T ENSP00000432330.1:n.188-428G>T
ENST00000528013.6:c.955+39G>T ENSP00000433130.2:n.955+39G>T
ENST00000529892.5:c.177+39G>T
ENST00000529984.5:c.188-428G>T ENSP00000437093.1:n.188-428G>T
ENST00000531105.5:c.115+2407G>T ENSP00000431292.1:n.115+2407G>T
ENST00000533178.5:c.542+39G>T ENSP00000436430.1:n.542+39G>T
NM_001048171.1:c.955+39G>T NP_001041636.1:n.955+39G>T
NM_001048172.1:c.916+39G>T NP_001041637.1:n.916+39G>T
NM_001048173.1:c.913+39G>T NP_001041638.1:n.913+39G>T
NM_001048174.1:c.913+39G>T NP_001041639.1:n.913+39G>T
NM_001128425.1:c.997+39G>T , LRG_220t1:c.997+39G>T NP_001121897.1:n.997+39G>T
NM_001293190.1:c.958+39G>T NP_001280119.1:n.958+39G>T
NM_001293191.1:c.946+39G>T NP_001280120.1:n.946+39G>T
NM_001293192.1:c.637+39G>T NP_001280121.1:n.637+39G>T
NM_001293195.1:c.913+39G>T NP_001280124.1:n.913+39G>T
NM_001293196.1:c.637+39G>T NP_001280125.1:n.637+39G>T
NM_012222.2:c.988+39G>T NP_036354.1:n.988+39G>T
XM_011541497.1:c.973+39G>T XP_011539799.1:n.973+39G>T
XM_011541498.1:c.955+39G>T XP_011539800.1:n.955+39G>T
XM_011541499.1:c.955+39G>T XP_011539801.1:n.955+39G>T
XM_011541500.1:c.955+39G>T XP_011539802.1:n.955+39G>T
XM_011541501.1:c.955+39G>T XP_011539803.1:n.955+39G>T
XM_011541502.1:c.955+39G>T XP_011539804.1:n.955+39G>T
XM_011541503.1:c.955+39G>T XP_011539805.1:n.955+39G>T
XM_011541504.1:c.946+39G>T XP_011539806.1:n.946+39G>T
XM_011541505.1:c.535+39G>T XP_011539807.1:n.535+39G>T
XM_011541506.1:c.535+39G>T XP_011539808.1:n.535+39G>T
XM_011541507.1:c.526+39G>T XP_011539809.1:n.526+39G>T
XM_011541508.1:c.541+39G>T XP_011539810.1:n.541+39G>T
XR_946658.1:n.1044+39G>T
NM_001350650.1:c.568+39G>T NP_001337579.1:n.568+39G>T
NM_001350651.1:c.568+39G>T NP_001337580.1:n.568+39G>T
NR_146882.1:n.1171+39G>T
NR_146883.1:n.985+39G>T
XM_011541497.3:c.973+39G>T XP_011539799.1:n.973+39G>T
XM_011541500.3:c.955+39G>T XP_011539802.1:n.955+39G>T
XM_011541501.2:c.955+39G>T XP_011539803.1:n.955+39G>T
XM_011541502.2:c.955+39G>T XP_011539804.1:n.955+39G>T
XM_011541503.2:c.955+39G>T XP_011539805.1:n.955+39G>T
XM_011541504.2:c.946+39G>T XP_011539806.1:n.946+39G>T
XM_011541505.2:c.535+39G>T XP_011539807.1:n.535+39G>T
XM_011541506.2:c.535+39G>T XP_011539808.1:n.535+39G>T
XM_017001331.1:c.955+39G>T XP_016856820.1:n.955+39G>T
XM_017001332.1:c.955+39G>T XP_016856821.1:n.955+39G>T
XM_017001333.1:c.955+39G>T XP_016856822.1:n.955+39G>T
XM_017001334.1:c.916+39G>T XP_016856823.1:n.916+39G>T
XM_017001335.1:c.637+39G>T XP_016856824.1:n.637+39G>T
XM_017001336.1:c.568+39G>T XP_016856825.1:n.568+39G>T
XM_017001337.1:c.568+39G>T XP_016856826.1:n.568+39G>T
XM_024447244.1:c.568+39G>T XP_024303012.1:n.568+39G>T
XM_024447245.1:c.568+39G>T XP_024303013.1:n.568+39G>T
XM_024447248.1:c.526+39G>T XP_024303016.1:n.526+39G>T
XM_024447249.1:c.397+39G>T XP_024303017.1:n.397+39G>T
XM_024447250.1:c.397+39G>T XP_024303018.1:n.397+39G>T
XM_024447251.1:c.397+39G>T XP_024303019.1:n.397+39G>T
XR_001737190.1:n.958+39G>T
XR_001737192.1:n.770+39G>T
XR_002956643.1:n.950+39G>T
XR_002956644.1:n.1485+39G>T
XR_946658.2:n.1058+39G>T
NM_001048171.2:c.913+39G>T NP_001041636.2:n.913+39G>T
NM_001128425.2:c.997+39G>T MANE Plus Clinical NP_001121897.1:n.997+39G>T
NM_001048172.2:c.916+39G>T NP_001041637.1:n.916+39G>T
NM_001048173.2:c.913+39G>T NP_001041638.1:n.913+39G>T
NM_001048174.2:c.913+39G>T MANE Select NP_001041639.1:n.913+39G>T
NM_001293190.2:c.958+39G>T NP_001280119.1:n.958+39G>T
NM_001293191.2:c.946+39G>T NP_001280120.1:n.946+39G>T
NM_001293192.2:c.637+39G>T NP_001280121.1:n.637+39G>T
NM_001293195.2:c.913+39G>T NP_001280124.1:n.913+39G>T
NM_001293196.2:c.637+39G>T NP_001280125.1:n.637+39G>T
NM_001350650.2:c.568+39G>T NP_001337579.1:n.568+39G>T
NM_001350651.2:c.568+39G>T NP_001337580.1:n.568+39G>T
NM_012222.3:c.988+39G>T NP_036354.1:n.988+39G>T
NR_146882.2:n.1141+39G>T
NR_146883.2:n.990+39G>T
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