Canonical Allele Identifier: CA340132462
Gene: MUTYH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331183T>A , CM000663.2:g.45331183T>A GRCh38
NC_000001.10:g.45796855T>A , CM000663.1:g.45796855T>A GRCh37
NC_000001.9:g.45569442T>A NCBI36
NG_008189.1:g.14288A>T , LRG_220:g.14288A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.1007A>T ENSP00000410263.2:p.Lys336Met
ENST00000435155.2:c.1424A>T ENSP00000403655.2:p.Lys475Met
ENST00000467459.6:c.*253A>T ENSP00000435889.2:n.*253A>T
ENST00000483127.2:c.1409A>T ENSP00000436469.2:p.Lys470Met
ENST00000485271.6:c.1391A>T ENSP00000431264.2:p.Lys464Met
ENST00000529892.6:c.1244A>T ENSP00000432528.2:p.Lys415Met
ENST00000533178.6:c.*720A>T ENSP00000436430.2:n.*720A>T
ENST00000672314.2:c.1391A>T ENSP00000500828.2:p.Lys464Met
ENST00000710952.2:c.1475A>T MANE Plus Clinical ENSP00000518552.2:p.Lys492Met
ENST00000672818.3:c.1466A>T ENSP00000500891.1:p.Lys489Met
ENST00000456914.7:c.1391A>T MANE Select ENSP00000407590.2:p.Lys464Met
ENST00000671898.1:c.1979A>T ENSP00000499896.1:p.Lys660Met
ENST00000672011.1:c.*720A>T ENSP00000500418.1:n.*720A>T
ENST00000672314.1:c.1391A>T ENSP00000500828.1:p.Lys464Met
ENST00000672818.2:c.1466A>T ENSP00000500891.1:p.Lys489Met
ENST00000673134.1:c.*1088A>T ENSP00000500526.1:n.*1088A>T
ENST00000354383.10:c.1394A>T ENSP00000346354.6:p.Lys465Met
ENST00000355498.6:c.1391A>T ENSP00000347685.2:p.Lys464Met
ENST00000372098.7:c.1466A>T ENSP00000361170.3:p.Lys489Met
ENST00000372104.5:c.1391A>T ENSP00000361176.1:p.Lys464Met
ENST00000372110.7:c.1436A>T ENSP00000361182.3:p.Lys479Met
ENST00000372115.7:c.1433A>T ENSP00000361187.3:p.Lys478Met
ENST00000448481.5:c.1424A>T ENSP00000409718.1:p.Lys475Met
ENST00000450313.5:c.1475A>T ENSP00000408176.1:p.Lys492Met
ENST00000456914.6:c.1391A>T ENSP00000407590.2:p.Lys464Met
ENST00000467459.5:c.808A>T ENSP00000435889.1:n.808A>T
ENST00000475516.5:c.*1204A>T ENSP00000433843.1:n.*1204A>T
ENST00000481571.5:c.*1204A>T ENSP00000436597.1:n.*1204A>T
ENST00000482094.5:n.712A>T
ENST00000485271.5:c.88A>T
ENST00000488731.6:c.476A>T ENSP00000432330.1:p.Lys159Met
ENST00000528013.6:c.1433A>T ENSP00000433130.2:p.Lys478Met
ENST00000529892.5:c.466A>T
ENST00000529984.5:c.476A>T ENSP00000437093.1:p.Lys159Met
ENST00000531105.5:c.116-1746A>T ENSP00000431292.1:n.116-1746A>T
ENST00000533178.5:c.1020A>T ENSP00000436430.1:n.1020A>T
NM_001048171.1:c.1433A>T NP_001041636.1:p.Lys478Met
NM_001048172.1:c.1394A>T NP_001041637.1:p.Lys465Met
NM_001048173.1:c.1391A>T NP_001041638.1:p.Lys464Met
NM_001048174.1:c.1391A>T NP_001041639.1:p.Lys464Met
NM_001128425.1:c.1475A>T , LRG_220t1:c.1475A>T NP_001121897.1:p.Lys492Met
NM_001293190.1:c.1436A>T NP_001280119.1:p.Lys479Met
NM_001293191.1:c.1424A>T NP_001280120.1:p.Lys475Met
NM_001293192.1:c.1115A>T NP_001280121.1:p.Lys372Met
NM_001293195.1:c.1391A>T NP_001280124.1:p.Lys464Met
NM_001293196.1:c.1115A>T NP_001280125.1:p.Lys372Met
NM_012222.2:c.1466A>T NP_036354.1:p.Lys489Met
XM_011541497.1:c.1451A>T XP_011539799.1:p.Lys484Met
XM_011541498.1:c.1433A>T XP_011539800.1:p.Lys478Met
XM_011541499.1:c.1433A>T XP_011539801.1:p.Lys478Met
XM_011541500.1:c.1433A>T XP_011539802.1:p.Lys478Met
XM_011541501.1:c.1433A>T XP_011539803.1:p.Lys478Met
XM_011541502.1:c.1433A>T XP_011539804.1:p.Lys478Met
XM_011541503.1:c.1433A>T XP_011539805.1:p.Lys478Met
XM_011541504.1:c.1424A>T XP_011539806.1:p.Lys475Met
XM_011541505.1:c.1013A>T XP_011539807.1:p.Lys338Met
XM_011541506.1:c.1013A>T XP_011539808.1:p.Lys338Met
XM_011541507.1:c.1004A>T XP_011539809.1:p.Lys335Met
XM_011541508.1:c.1019A>T XP_011539810.1:p.Lys340Met
XR_946658.1:n.1522A>T
NM_001350650.1:c.1046A>T NP_001337579.1:p.Lys349Met
NM_001350651.1:c.1046A>T NP_001337580.1:p.Lys349Met
NR_146882.1:n.1649A>T
NR_146883.1:n.1463A>T
XM_011541497.3:c.1451A>T XP_011539799.1:p.Lys484Met
XM_011541500.3:c.1433A>T XP_011539802.1:p.Lys478Met
XM_011541501.2:c.1433A>T XP_011539803.1:p.Lys478Met
XM_011541502.2:c.1433A>T XP_011539804.1:p.Lys478Met
XM_011541503.2:c.1433A>T XP_011539805.1:p.Lys478Met
XM_011541504.2:c.1424A>T XP_011539806.1:p.Lys475Met
XM_011541505.2:c.1013A>T XP_011539807.1:p.Lys338Met
XM_011541506.2:c.1013A>T XP_011539808.1:p.Lys338Met
XM_017001331.1:c.1433A>T XP_016856820.1:p.Lys478Met
XM_017001332.1:c.1433A>T XP_016856821.1:p.Lys478Met
XM_017001333.1:c.1433A>T XP_016856822.1:p.Lys478Met
XM_017001334.1:c.1394A>T XP_016856823.1:p.Lys465Met
XM_017001335.1:c.1115A>T XP_016856824.1:p.Lys372Met
XM_017001336.1:c.1046A>T XP_016856825.1:p.Lys349Met
XM_017001337.1:c.1046A>T XP_016856826.1:p.Lys349Met
XM_024447244.1:c.1046A>T XP_024303012.1:p.Lys349Met
XM_024447245.1:c.1046A>T XP_024303013.1:p.Lys349Met
XM_024447248.1:c.1004A>T XP_024303016.1:p.Lys335Met
XM_024447249.1:c.875A>T XP_024303017.1:p.Lys292Met
XM_024447250.1:c.875A>T XP_024303018.1:p.Lys292Met
XM_024447251.1:c.875A>T XP_024303019.1:p.Lys292Met
XR_001737190.1:n.1436A>T
XR_001737192.1:n.1248A>T
XR_002956643.1:n.1428A>T
XR_002956644.1:n.1963A>T
XR_946658.2:n.1536A>T
NM_001048171.2:c.1391A>T NP_001041636.2:p.Lys464Met
NM_001128425.2:c.1475A>T MANE Plus Clinical NP_001121897.1:p.Lys492Met
NM_001048172.2:c.1394A>T NP_001041637.1:p.Lys465Met
NM_001048173.2:c.1391A>T NP_001041638.1:p.Lys464Met
NM_001048174.2:c.1391A>T MANE Select NP_001041639.1:p.Lys464Met
NM_001293190.2:c.1436A>T NP_001280119.1:p.Lys479Met
NM_001293191.2:c.1424A>T NP_001280120.1:p.Lys475Met
NM_001293192.2:c.1115A>T NP_001280121.1:p.Lys372Met
NM_001293195.2:c.1391A>T NP_001280124.1:p.Lys464Met
NM_001293196.2:c.1115A>T NP_001280125.1:p.Lys372Met
NM_001350650.2:c.1046A>T NP_001337579.1:p.Lys349Met
NM_001350651.2:c.1046A>T NP_001337580.1:p.Lys349Met
NM_012222.3:c.1466A>T NP_036354.1:p.Lys489Met
NR_146882.2:n.1619A>T
NR_146883.2:n.1468A>T