Canonical Allele Identifier: CA915941260

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 818740
• ClinVar RCV Id: RCV001010634
• dbSNP Id: rs1570373385

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331477del , CM000663.2:g.45331477del	GRCh38
NC_000001.10:g.45797149del , CM000663.1:g.45797149del	GRCh37
NC_000001.9:g.45569736del	NCBI36
NG_008189.1:g.13995del , LRG_220:g.13995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.799del	ENSP00000410263.2:p.Glu267AsnfsTer29
ENST00000435155.2:c.1216del	ENSP00000403655.2:p.Glu406AsnfsTer29
ENST00000467459.6:c.*45del	ENSP00000435889.2:n.*45del
ENST00000483127.2:c.1201del	ENSP00000436469.2:p.Glu401AsnfsTer29
ENST00000485271.6:c.1183del	ENSP00000431264.2:p.Glu395AsnfsTer29
ENST00000529892.6:c.1036del	ENSP00000432528.2:p.Glu346AsnfsTer29
ENST00000533178.6:c.*512del	ENSP00000436430.2:n.*512del
ENST00000672314.2:c.1183del	ENSP00000500828.2:p.Glu395AsnfsTer29
ENST00000710952.2:c.1267del MANE Plus Clinical	ENSP00000518552.2:p.Glu423AsnfsTer29
ENST00000672818.3:c.1258del	ENSP00000500891.1:p.Glu420AsnfsTer29
ENST00000456914.7:c.1183del MANE Select	ENSP00000407590.2:p.Glu395AsnfsTer29
ENST00000671898.1:c.1771del	ENSP00000499896.1:p.Glu591AsnfsTer29
ENST00000672011.1:c.*512del	ENSP00000500418.1:n.*512del
ENST00000672314.1:c.1183del	ENSP00000500828.1:p.Glu395AsnfsTer29
ENST00000672593.1:c.*1409del	ENSP00000500455.1:n.*1409del
ENST00000672818.2:c.1258del	ENSP00000500891.1:p.Glu420AsnfsTer29
ENST00000673134.1:c.*880del	ENSP00000500526.1:n.*880del
ENST00000354383.10:c.1186del	ENSP00000346354.6:p.Glu396AsnfsTer29
ENST00000355498.6:c.1183del	ENSP00000347685.2:p.Glu395AsnfsTer29
ENST00000372098.7:c.1258del	ENSP00000361170.3:p.Glu420AsnfsTer29
ENST00000372104.5:c.1183del	ENSP00000361176.1:p.Glu395AsnfsTer29
ENST00000372110.7:c.1228del	ENSP00000361182.3:p.Glu410AsnfsTer29
ENST00000372115.7:c.1225del	ENSP00000361187.3:p.Glu409AsnfsTer29
ENST00000448481.5:c.1216del	ENSP00000409718.1:p.Glu406AsnfsTer29
ENST00000450313.5:c.1267del	ENSP00000408176.1:p.Glu423AsnfsTer29
ENST00000456914.6:c.1183del	ENSP00000407590.2:p.Glu395AsnfsTer29
ENST00000467459.5:c.600del	ENSP00000435889.1:n.600del
ENST00000475516.5:c.*996del	ENSP00000433843.1:n.*996del
ENST00000481571.5:c.*996del	ENSP00000436597.1:n.*996del
ENST00000482094.5:n.504del
ENST00000488731.6:c.268del	ENSP00000432330.1:p.Glu90AsnfsTer29
ENST00000528013.6:c.1225del	ENSP00000433130.2:p.Glu409AsnfsTer29
ENST00000529892.5:c.258del
ENST00000529984.5:c.268del	ENSP00000437093.1:p.Glu90AsnfsTer29
ENST00000531105.5:c.116-2039del	ENSP00000431292.1:n.116-2039del
ENST00000533178.5:c.812del	ENSP00000436430.1:n.812del
NM_001048171.1:c.1225del	NP_001041636.1:p.Glu409AsnfsTer29
NM_001048172.1:c.1186del	NP_001041637.1:p.Glu396AsnfsTer29
NM_001048173.1:c.1183del	NP_001041638.1:p.Glu395AsnfsTer29
NM_001048174.1:c.1183del	NP_001041639.1:p.Glu395AsnfsTer29
NM_001128425.1:c.1267del , LRG_220t1:c.1267del	NP_001121897.1:p.Glu423AsnfsTer29
NM_001293190.1:c.1228del	NP_001280119.1:p.Glu410AsnfsTer29
NM_001293191.1:c.1216del	NP_001280120.1:p.Glu406AsnfsTer29
NM_001293192.1:c.907del	NP_001280121.1:p.Glu303AsnfsTer29
NM_001293195.1:c.1183del	NP_001280124.1:p.Glu395AsnfsTer29
NM_001293196.1:c.907del	NP_001280125.1:p.Glu303AsnfsTer29
NM_012222.2:c.1258del	NP_036354.1:p.Glu420AsnfsTer29
XM_011541497.1:c.1243del	XP_011539799.1:p.Glu415AsnfsTer29
XM_011541498.1:c.1225del	XP_011539800.1:p.Glu409AsnfsTer29
XM_011541499.1:c.1225del	XP_011539801.1:p.Glu409AsnfsTer29
XM_011541500.1:c.1225del	XP_011539802.1:p.Glu409AsnfsTer29
XM_011541501.1:c.1225del	XP_011539803.1:p.Glu409AsnfsTer29
XM_011541502.1:c.1225del	XP_011539804.1:p.Glu409AsnfsTer29
XM_011541503.1:c.1225del	XP_011539805.1:p.Glu409AsnfsTer29
XM_011541504.1:c.1216del	XP_011539806.1:p.Glu406AsnfsTer29
XM_011541505.1:c.805del	XP_011539807.1:p.Glu269AsnfsTer29
XM_011541506.1:c.805del	XP_011539808.1:p.Glu269AsnfsTer29
XM_011541507.1:c.796del	XP_011539809.1:p.Glu266AsnfsTer29
XM_011541508.1:c.811del	XP_011539810.1:p.Glu271AsnfsTer29
XR_946658.1:n.1314del
NM_001350650.1:c.838del	NP_001337579.1:p.Glu280AsnfsTer29
NM_001350651.1:c.838del	NP_001337580.1:p.Glu280AsnfsTer29
NR_146882.1:n.1441del
NR_146883.1:n.1255del
XM_011541497.3:c.1243del	XP_011539799.1:p.Glu415AsnfsTer29
XM_011541500.3:c.1225del	XP_011539802.1:p.Glu409AsnfsTer29
XM_011541501.2:c.1225del	XP_011539803.1:p.Glu409AsnfsTer29
XM_011541502.2:c.1225del	XP_011539804.1:p.Glu409AsnfsTer29
XM_011541503.2:c.1225del	XP_011539805.1:p.Glu409AsnfsTer29
XM_011541504.2:c.1216del	XP_011539806.1:p.Glu406AsnfsTer29
XM_011541505.2:c.805del	XP_011539807.1:p.Glu269AsnfsTer29
XM_011541506.2:c.805del	XP_011539808.1:p.Glu269AsnfsTer29
XM_017001331.1:c.1225del	XP_016856820.1:p.Glu409AsnfsTer29
XM_017001332.1:c.1225del	XP_016856821.1:p.Glu409AsnfsTer29
XM_017001333.1:c.1225del	XP_016856822.1:p.Glu409AsnfsTer29
XM_017001334.1:c.1186del	XP_016856823.1:p.Glu396AsnfsTer29
XM_017001335.1:c.907del	XP_016856824.1:p.Glu303AsnfsTer29
XM_017001336.1:c.838del	XP_016856825.1:p.Glu280AsnfsTer29
XM_017001337.1:c.838del	XP_016856826.1:p.Glu280AsnfsTer29
XM_024447244.1:c.838del	XP_024303012.1:p.Glu280AsnfsTer29
XM_024447245.1:c.838del	XP_024303013.1:p.Glu280AsnfsTer29
XM_024447248.1:c.796del	XP_024303016.1:p.Glu266AsnfsTer29
XM_024447249.1:c.667del	XP_024303017.1:p.Glu223AsnfsTer29
XM_024447250.1:c.667del	XP_024303018.1:p.Glu223AsnfsTer29
XM_024447251.1:c.667del	XP_024303019.1:p.Glu223AsnfsTer29
XR_001737190.1:n.1228del
XR_001737192.1:n.1040del
XR_002956643.1:n.1220del
XR_002956644.1:n.1755del
XR_946658.2:n.1328del
NM_001048171.2:c.1183del	NP_001041636.2:p.Glu395AsnfsTer29
NM_001128425.2:c.1267del MANE Plus Clinical	NP_001121897.1:p.Glu423AsnfsTer29
NM_001048172.2:c.1186del	NP_001041637.1:p.Glu396AsnfsTer29
NM_001048173.2:c.1183del	NP_001041638.1:p.Glu395AsnfsTer29
NM_001048174.2:c.1183del MANE Select	NP_001041639.1:p.Glu395AsnfsTer29
NM_001293190.2:c.1228del	NP_001280119.1:p.Glu410AsnfsTer29
NM_001293191.2:c.1216del	NP_001280120.1:p.Glu406AsnfsTer29
NM_001293192.2:c.907del	NP_001280121.1:p.Glu303AsnfsTer29
NM_001293195.2:c.1183del	NP_001280124.1:p.Glu395AsnfsTer29
NM_001293196.2:c.907del	NP_001280125.1:p.Glu303AsnfsTer29
NM_001350650.2:c.838del	NP_001337579.1:p.Glu280AsnfsTer29
NM_001350651.2:c.838del	NP_001337580.1:p.Glu280AsnfsTer29
NM_012222.3:c.1258del	NP_036354.1:p.Glu420AsnfsTer29
NR_146882.2:n.1411del
NR_146883.2:n.1260del