Canonical Allele Identifier: CA417702072
Gene: MUTYH HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45796914A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331242A>C , CM000663.2:g.45331242A>C GRCh38
NC_000001.10:g.45796914A>C , CM000663.1:g.45796914A>C GRCh37
NC_000001.9:g.45569501A>C NCBI36
NG_008189.1:g.14229T>G , LRG_220:g.14229T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000672818.3:c.1407T>G ENSP00000500891.1:p.Gly469=
ENST00000456914.7:c.1332T>G MANE Select ENSP00000407590.2:p.Gly444=
ENST00000671898.1:c.1920T>G ENSP00000499896.1:p.Gly640=
ENST00000672011.1:c.*661T>G ENSP00000500418.1:n.*661T>G
ENST00000672314.1:c.1332T>G ENSP00000500828.1:p.Gly444=
ENST00000672818.2:c.1407T>G ENSP00000500891.1:p.Gly469=
ENST00000673134.1:c.*1029T>G ENSP00000500526.1:n.*1029T>G
ENST00000354383.10:c.1335T>G ENSP00000346354.6:p.Gly445=
ENST00000355498.6:c.1332T>G ENSP00000347685.2:p.Gly444=
ENST00000372098.7:c.1407T>G ENSP00000361170.3:p.Gly469=
ENST00000372104.5:c.1332T>G ENSP00000361176.1:p.Gly444=
ENST00000372110.7:c.1377T>G ENSP00000361182.3:p.Gly459=
ENST00000372115.7:c.1374T>G ENSP00000361187.3:p.Gly458=
ENST00000448481.5:c.1365T>G ENSP00000409718.1:p.Gly455=
ENST00000450313.5:c.1416T>G ENSP00000408176.1:p.Gly472=
ENST00000456914.6:c.1332T>G ENSP00000407590.2:p.Gly444=
ENST00000467459.5:n.749T>G ENSP00000435889.1:n.749T>G
ENST00000475516.5:c.*1145T>G ENSP00000433843.1:n.*1145T>G
ENST00000481571.5:c.*1145T>G ENSP00000436597.1:n.*1145T>G
ENST00000482094.5:n.653T>G
ENST00000485271.5:n.29T>G
ENST00000488731.6:c.417T>G ENSP00000432330.1:p.Gly139=
ENST00000528013.6:c.1374T>G ENSP00000433130.2:p.Gly458=
ENST00000529892.5:n.407T>G
ENST00000529984.5:c.417T>G ENSP00000437093.1:p.Gly139=
ENST00000531105.5:c.116-1805T>G ENSP00000431292.1:n.116-1805T>G
ENST00000533178.5:n.961T>G ENSP00000436430.1:n.961T>G
NM_001048171.1:c.1374T>G NP_001041636.1:p.Gly458=
NM_001048172.1:c.1335T>G NP_001041637.1:p.Gly445=
NM_001048173.1:c.1332T>G NP_001041638.1:p.Gly444=
NM_001048174.1:c.1332T>G NP_001041639.1:p.Gly444=
NM_001128425.1:c.1416T>G , LRG_220t1:c.1416T>G NP_001121897.1:p.Gly472=
NM_001293190.1:c.1377T>G NP_001280119.1:p.Gly459=
NM_001293191.1:c.1365T>G NP_001280120.1:p.Gly455=
NM_001293192.1:c.1056T>G NP_001280121.1:p.Gly352=
NM_001293195.1:c.1332T>G NP_001280124.1:p.Gly444=
NM_001293196.1:c.1056T>G NP_001280125.1:p.Gly352=
NM_012222.2:c.1407T>G NP_036354.1:p.Gly469=
XM_011541497.1:c.1392T>G XP_011539799.1:p.Gly464=
XM_011541498.1:c.1374T>G XP_011539800.1:p.Gly458=
XM_011541499.1:c.1374T>G XP_011539801.1:p.Gly458=
XM_011541500.1:c.1374T>G XP_011539802.1:p.Gly458=
XM_011541501.1:c.1374T>G XP_011539803.1:p.Gly458=
XM_011541502.1:c.1374T>G XP_011539804.1:p.Gly458=
XM_011541503.1:c.1374T>G XP_011539805.1:p.Gly458=
XM_011541504.1:c.1365T>G XP_011539806.1:p.Gly455=
XM_011541505.1:c.954T>G XP_011539807.1:p.Gly318=
XM_011541506.1:c.954T>G XP_011539808.1:p.Gly318=
XM_011541507.1:c.945T>G XP_011539809.1:p.Gly315=
XM_011541508.1:c.960T>G XP_011539810.1:p.Gly320=
XR_946658.1:n.1463T>G
NM_001350650.1:c.987T>G NP_001337579.1:p.Gly329=
NM_001350651.1:c.987T>G NP_001337580.1:p.Gly329=
NR_146882.1:n.1590T>G
NR_146883.1:n.1404T>G
XM_011541497.3:c.1392T>G XP_011539799.1:p.Gly464=
XM_011541500.3:c.1374T>G XP_011539802.1:p.Gly458=
XM_011541501.2:c.1374T>G XP_011539803.1:p.Gly458=
XM_011541502.2:c.1374T>G XP_011539804.1:p.Gly458=
XM_011541503.2:c.1374T>G XP_011539805.1:p.Gly458=
XM_011541504.2:c.1365T>G XP_011539806.1:p.Gly455=
XM_011541505.2:c.954T>G XP_011539807.1:p.Gly318=
XM_011541506.2:c.954T>G XP_011539808.1:p.Gly318=
XM_017001331.1:c.1374T>G XP_016856820.1:p.Gly458=
XM_017001332.1:c.1374T>G XP_016856821.1:p.Gly458=
XM_017001333.1:c.1374T>G XP_016856822.1:p.Gly458=
XM_017001334.1:c.1335T>G XP_016856823.1:p.Gly445=
XM_017001335.1:c.1056T>G XP_016856824.1:p.Gly352=
XM_017001336.1:c.987T>G XP_016856825.1:p.Gly329=
XM_017001337.1:c.987T>G XP_016856826.1:p.Gly329=
XM_024447244.1:c.987T>G XP_024303012.1:p.Gly329=
XM_024447245.1:c.987T>G XP_024303013.1:p.Gly329=
XM_024447248.1:c.945T>G XP_024303016.1:p.Gly315=
XM_024447249.1:c.816T>G XP_024303017.1:p.Gly272=
XM_024447250.1:c.816T>G XP_024303018.1:p.Gly272=
XM_024447251.1:c.816T>G XP_024303019.1:p.Gly272=
XR_001737190.1:n.1377T>G
XR_001737192.1:n.1189T>G
XR_002956643.1:n.1369T>G
XR_002956644.1:n.1904T>G
XR_946658.2:n.1477T>G
NM_001048171.2:c.1332T>G NP_001041636.2:p.Gly444=
NM_001128425.2:c.1416T>G NP_001121897.1:p.Gly472=
NM_001048172.2:c.1335T>G NP_001041637.1:p.Gly445=
NM_001048173.2:c.1332T>G NP_001041638.1:p.Gly444=
NM_001048174.2:c.1332T>G MANE Select NP_001041639.1:p.Gly444=
NM_001293190.2:c.1377T>G NP_001280119.1:p.Gly459=
NM_001293191.2:c.1365T>G NP_001280120.1:p.Gly455=
NM_001293192.2:c.1056T>G NP_001280121.1:p.Gly352=
NM_001293195.2:c.1332T>G NP_001280124.1:p.Gly444=
NM_001293196.2:c.1056T>G NP_001280125.1:p.Gly352=
NM_001350650.2:c.987T>G NP_001337579.1:p.Gly329=
NM_001350651.2:c.987T>G NP_001337580.1:p.Gly329=
NM_012222.3:c.1407T>G NP_036354.1:p.Gly469=
NR_146882.2:n.1560T>G
NR_146883.2:n.1409T>G