Canonical Allele Identifier: CA340133089

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45797201G>C (hg19) ; chr1:g.45331529G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331529G>C , CM000663.2:g.45331529G>C	GRCh38
NC_000001.10:g.45797201G>C , CM000663.1:g.45797201G>C	GRCh37
NC_000001.9:g.45569788G>C	NCBI36
NG_008189.1:g.13942C>G , LRG_220:g.13942C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.746C>G	ENSP00000410263.2:p.Pro249Arg
ENST00000435155.2:c.1163C>G	ENSP00000403655.2:p.Pro388Arg
ENST00000467459.6:c.1153C>G	ENSP00000435889.2:p.Arg385Gly
ENST00000483127.2:c.1148C>G	ENSP00000436469.2:p.Pro383Arg
ENST00000485271.6:c.1130C>G	ENSP00000431264.2:p.Pro377Arg
ENST00000529892.6:c.983C>G	ENSP00000432528.2:p.Pro328Arg
ENST00000533178.6:c.*459C>G	ENSP00000436430.2:n.*459C>G
ENST00000672314.2:c.1130C>G	ENSP00000500828.2:p.Pro377Arg
ENST00000710952.2:c.1214C>G MANE Plus Clinical	ENSP00000518552.2:p.Pro405Arg
ENST00000672818.3:c.1205C>G	ENSP00000500891.1:p.Pro402Arg
ENST00000456914.7:c.1130C>G MANE Select	ENSP00000407590.2:p.Pro377Arg
ENST00000671898.1:c.1718C>G	ENSP00000499896.1:p.Pro573Arg
ENST00000672011.1:c.*459C>G	ENSP00000500418.1:n.*459C>G
ENST00000672314.1:c.1130C>G	ENSP00000500828.1:p.Pro377Arg
ENST00000672593.1:c.*1356C>G	ENSP00000500455.1:n.*1356C>G
ENST00000672818.2:c.1205C>G	ENSP00000500891.1:p.Pro402Arg
ENST00000673134.1:c.*827C>G	ENSP00000500526.1:n.*827C>G
ENST00000354383.10:c.1133C>G	ENSP00000346354.6:p.Pro378Arg
ENST00000355498.6:c.1130C>G	ENSP00000347685.2:p.Pro377Arg
ENST00000372098.7:c.1205C>G	ENSP00000361170.3:p.Pro402Arg
ENST00000372104.5:c.1130C>G	ENSP00000361176.1:p.Pro377Arg
ENST00000372110.7:c.1175C>G	ENSP00000361182.3:p.Pro392Arg
ENST00000372115.7:c.1172C>G	ENSP00000361187.3:p.Pro391Arg
ENST00000448481.5:c.1163C>G	ENSP00000409718.1:p.Pro388Arg
ENST00000450313.5:c.1214C>G	ENSP00000408176.1:p.Pro405Arg
ENST00000456914.6:c.1130C>G	ENSP00000407590.2:p.Pro377Arg
ENST00000467459.5:c.547C>G	ENSP00000435889.1:p.Arg183Gly
ENST00000475516.5:c.*943C>G	ENSP00000433843.1:n.*943C>G
ENST00000481571.5:c.*943C>G	ENSP00000436597.1:n.*943C>G
ENST00000482094.5:n.451C>G
ENST00000488731.6:c.215C>G	ENSP00000432330.1:p.Pro72Arg
ENST00000528013.6:c.1172C>G	ENSP00000433130.2:p.Pro391Arg
ENST00000529892.5:c.205C>G
ENST00000529984.5:c.215C>G	ENSP00000437093.1:p.Pro72Arg
ENST00000531105.5:c.116-2092C>G	ENSP00000431292.1:n.116-2092C>G
ENST00000533178.5:c.759C>G	ENSP00000436430.1:n.759C>G
NM_001048171.1:c.1172C>G	NP_001041636.1:p.Pro391Arg
NM_001048172.1:c.1133C>G	NP_001041637.1:p.Pro378Arg
NM_001048173.1:c.1130C>G	NP_001041638.1:p.Pro377Arg
NM_001048174.1:c.1130C>G	NP_001041639.1:p.Pro377Arg
NM_001128425.1:c.1214C>G , LRG_220t1:c.1214C>G	NP_001121897.1:p.Pro405Arg
NM_001293190.1:c.1175C>G	NP_001280119.1:p.Pro392Arg
NM_001293191.1:c.1163C>G	NP_001280120.1:p.Pro388Arg
NM_001293192.1:c.854C>G	NP_001280121.1:p.Pro285Arg
NM_001293195.1:c.1130C>G	NP_001280124.1:p.Pro377Arg
NM_001293196.1:c.854C>G	NP_001280125.1:p.Pro285Arg
NM_012222.2:c.1205C>G	NP_036354.1:p.Pro402Arg
XM_011541497.1:c.1190C>G	XP_011539799.1:p.Pro397Arg
XM_011541498.1:c.1172C>G	XP_011539800.1:p.Pro391Arg
XM_011541499.1:c.1172C>G	XP_011539801.1:p.Pro391Arg
XM_011541500.1:c.1172C>G	XP_011539802.1:p.Pro391Arg
XM_011541501.1:c.1172C>G	XP_011539803.1:p.Pro391Arg
XM_011541502.1:c.1172C>G	XP_011539804.1:p.Pro391Arg
XM_011541503.1:c.1172C>G	XP_011539805.1:p.Pro391Arg
XM_011541504.1:c.1163C>G	XP_011539806.1:p.Pro388Arg
XM_011541505.1:c.752C>G	XP_011539807.1:p.Pro251Arg
XM_011541506.1:c.752C>G	XP_011539808.1:p.Pro251Arg
XM_011541507.1:c.743C>G	XP_011539809.1:p.Pro248Arg
XM_011541508.1:c.758C>G	XP_011539810.1:p.Pro253Arg
XR_946658.1:n.1261C>G
NM_001350650.1:c.785C>G	NP_001337579.1:p.Pro262Arg
NM_001350651.1:c.785C>G	NP_001337580.1:p.Pro262Arg
NR_146882.1:n.1388C>G
NR_146883.1:n.1202C>G
XM_011541497.3:c.1190C>G	XP_011539799.1:p.Pro397Arg
XM_011541500.3:c.1172C>G	XP_011539802.1:p.Pro391Arg
XM_011541501.2:c.1172C>G	XP_011539803.1:p.Pro391Arg
XM_011541502.2:c.1172C>G	XP_011539804.1:p.Pro391Arg
XM_011541503.2:c.1172C>G	XP_011539805.1:p.Pro391Arg
XM_011541504.2:c.1163C>G	XP_011539806.1:p.Pro388Arg
XM_011541505.2:c.752C>G	XP_011539807.1:p.Pro251Arg
XM_011541506.2:c.752C>G	XP_011539808.1:p.Pro251Arg
XM_017001331.1:c.1172C>G	XP_016856820.1:p.Pro391Arg
XM_017001332.1:c.1172C>G	XP_016856821.1:p.Pro391Arg
XM_017001333.1:c.1172C>G	XP_016856822.1:p.Pro391Arg
XM_017001334.1:c.1133C>G	XP_016856823.1:p.Pro378Arg
XM_017001335.1:c.854C>G	XP_016856824.1:p.Pro285Arg
XM_017001336.1:c.785C>G	XP_016856825.1:p.Pro262Arg
XM_017001337.1:c.785C>G	XP_016856826.1:p.Pro262Arg
XM_024447244.1:c.785C>G	XP_024303012.1:p.Pro262Arg
XM_024447245.1:c.785C>G	XP_024303013.1:p.Pro262Arg
XM_024447248.1:c.743C>G	XP_024303016.1:p.Pro248Arg
XM_024447249.1:c.614C>G	XP_024303017.1:p.Pro205Arg
XM_024447250.1:c.614C>G	XP_024303018.1:p.Pro205Arg
XM_024447251.1:c.614C>G	XP_024303019.1:p.Pro205Arg
XR_001737190.1:n.1175C>G
XR_001737192.1:n.987C>G
XR_002956643.1:n.1167C>G
XR_002956644.1:n.1702C>G
XR_946658.2:n.1275C>G
NM_001048171.2:c.1130C>G	NP_001041636.2:p.Pro377Arg
NM_001128425.2:c.1214C>G MANE Plus Clinical	NP_001121897.1:p.Pro405Arg
NM_001048172.2:c.1133C>G	NP_001041637.1:p.Pro378Arg
NM_001048173.2:c.1130C>G	NP_001041638.1:p.Pro377Arg
NM_001048174.2:c.1130C>G MANE Select	NP_001041639.1:p.Pro377Arg
NM_001293190.2:c.1175C>G	NP_001280119.1:p.Pro392Arg
NM_001293191.2:c.1163C>G	NP_001280120.1:p.Pro388Arg
NM_001293192.2:c.854C>G	NP_001280121.1:p.Pro285Arg
NM_001293195.2:c.1130C>G	NP_001280124.1:p.Pro377Arg
NM_001293196.2:c.854C>G	NP_001280125.1:p.Pro285Arg
NM_001350650.2:c.785C>G	NP_001337579.1:p.Pro262Arg
NM_001350651.2:c.785C>G	NP_001337580.1:p.Pro262Arg
NM_012222.3:c.1205C>G	NP_036354.1:p.Pro402Arg
NR_146882.2:n.1358C>G
NR_146883.2:n.1207C>G