Canonical Allele Identifier: CA340137144
Gene: MUTYH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45334457C>A , CM000663.2:g.45334457C>A GRCh38
NC_000001.10:g.45800129C>A , CM000663.1:g.45800129C>A GRCh37
NC_000001.9:g.45572716C>A NCBI36
NG_008189.1:g.11014G>T , LRG_220:g.11014G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.37-1623G>T ENSP00000410263.2:n.37-1623G>T
ENST00000435155.2:c.49G>T ENSP00000403655.2:p.Ala17Ser
ENST00000467459.6:c.49G>T ENSP00000435889.2:p.Ala17Ser
ENST00000483127.2:c.67G>T ENSP00000436469.2:p.Ala23Ser
ENST00000485271.6:c.49G>T ENSP00000431264.2:p.Ala17Ser
ENST00000529892.6:c.91G>T ENSP00000432528.2:p.Ala31Ser
ENST00000533178.6:c.49G>T ENSP00000436430.2:p.Ala17Ser
ENST00000672314.2:c.49G>T ENSP00000500828.2:p.Ala17Ser
ENST00000674679.2:c.49G>T ENSP00000501623.2:p.Ala17Ser
ENST00000710952.2:c.91G>T MANE Plus Clinical ENSP00000518552.2:p.Ala31Ser
ENST00000672818.3:c.91G>T ENSP00000500891.1:p.Ala31Ser
ENST00000450313.6:c.91G>T ENSP00000408176.2:p.Ala31Ser
ENST00000456914.7:c.49G>T MANE Select ENSP00000407590.2:p.Ala17Ser
ENST00000461495.6:c.91G>T ENSP00000437166.1:p.Ala31Ser
ENST00000671856.1:n.69G>T
ENST00000671898.1:c.595G>T ENSP00000499896.1:p.Ala199Ser
ENST00000672011.1:c.91G>T ENSP00000500418.1:p.Ala31Ser
ENST00000672314.1:c.49G>T ENSP00000500828.1:p.Ala17Ser
ENST00000672593.1:c.49G>T ENSP00000500455.1:p.Ala17Ser
ENST00000672764.1:c.49G>T ENSP00000500886.1:p.Ala17Ser
ENST00000672818.2:c.91G>T ENSP00000500891.1:p.Ala31Ser
ENST00000673134.1:c.49G>T ENSP00000500526.1:p.Ala17Ser
ENST00000674679.1:c.21G>T ENSP00000501623.1:p.Gln7His
ENST00000354383.10:c.49G>T ENSP00000346354.6:p.Ala17Ser
ENST00000355498.6:c.49G>T ENSP00000347685.2:p.Ala17Ser
ENST00000372098.7:c.91G>T ENSP00000361170.3:p.Ala31Ser
ENST00000372104.5:c.49G>T ENSP00000361176.1:p.Ala17Ser
ENST00000372110.7:c.91G>T ENSP00000361182.3:p.Ala31Ser
ENST00000372115.7:c.91G>T ENSP00000361187.3:p.Ala31Ser
ENST00000412971.5:c.37-1623G>T ENSP00000410263.1:n.37-1623G>T
ENST00000435155.1:c.49G>T ENSP00000403655.1:p.Ala17Ser
ENST00000448481.5:c.49G>T ENSP00000409718.1:p.Ala17Ser
ENST00000450313.5:c.91G>T ENSP00000408176.1:p.Ala31Ser
ENST00000456914.6:c.49G>T ENSP00000407590.2:p.Ala17Ser
ENST00000461495.5:c.91G>T ENSP00000437166.1:p.Ala31Ser
ENST00000462387.5:n.269G>T
ENST00000467940.5:c.107G>T ENSP00000436478.1:p.Ser36Ile
ENST00000470256.5:c.49G>T ENSP00000434985.1:p.Ala17Ser
ENST00000474703.1:n.171G>T
ENST00000475516.5:c.49G>T ENSP00000433843.1:p.Ala17Ser
ENST00000476789.5:n.269G>T
ENST00000479746.6:n.112G>T
ENST00000481139.5:n.252G>T
ENST00000481571.5:c.91G>T ENSP00000436597.1:p.Ala31Ser
ENST00000483127.1:c.67G>T ENSP00000436469.1:p.Ala23Ser
ENST00000483642.5:n.230G>T
ENST00000485484.5:n.99G>T
ENST00000488731.6:c.49G>T ENSP00000432330.1:p.Ala17Ser
ENST00000492494.5:n.112G>T
ENST00000525160.5:c.91G>T ENSP00000431568.1:p.Ala31Ser
ENST00000528013.6:c.49G>T ENSP00000433130.2:p.Ala17Ser
ENST00000529984.5:c.49G>T ENSP00000437093.1:p.Ala17Ser
ENST00000531105.5:c.49G>T ENSP00000431292.1:p.Ala17Ser
ENST00000533178.5:c.55G>T ENSP00000436430.1:p.Ala19Ser
ENST00000534453.1:n.315G>T
NM_001048171.1:c.91G>T NP_001041636.1:p.Ala31Ser
NM_001048172.1:c.49G>T NP_001041637.1:p.Ala17Ser
NM_001048173.1:c.49G>T NP_001041638.1:p.Ala17Ser
NM_001048174.1:c.49G>T NP_001041639.1:p.Ala17Ser
NM_001128425.1:c.91G>T , LRG_220t1:c.91G>T NP_001121897.1:p.Ala31Ser
NM_001293190.1:c.91G>T NP_001280119.1:p.Ala31Ser
NM_001293191.1:c.49G>T NP_001280120.1:p.Ala17Ser
NM_001293192.1:c.-164G>T NP_001280121.1:n.-164G>T
NM_001293195.1:c.49G>T NP_001280124.1:p.Ala17Ser
NM_001293196.1:c.-164G>T NP_001280125.1:n.-164G>T
NM_012222.2:c.91G>T NP_036354.1:p.Ala31Ser
XM_011541497.1:c.67G>T XP_011539799.1:p.Ala23Ser
XM_011541498.1:c.49G>T XP_011539800.1:p.Ala17Ser
XM_011541499.1:c.49G>T XP_011539801.1:p.Ala17Ser
XM_011541500.1:c.49G>T XP_011539802.1:p.Ala17Ser
XM_011541501.1:c.49G>T XP_011539803.1:p.Ala17Ser
XM_011541502.1:c.49G>T XP_011539804.1:p.Ala17Ser
XM_011541503.1:c.91G>T XP_011539805.1:p.Ala31Ser
XM_011541504.1:c.49G>T XP_011539806.1:p.Ala17Ser
XM_011541505.1:c.-25G>T XP_011539807.1:n.-25G>T
XM_011541506.1:c.-25G>T XP_011539808.1:n.-25G>T
XR_946658.1:n.138G>T
NM_001350650.1:c.-223G>T NP_001337579.1:n.-223G>T
NM_001350651.1:c.-159G>T NP_001337580.1:n.-159G>T
NR_146882.1:n.307G>T
NR_146883.1:n.195G>T
XM_011541497.3:c.67G>T XP_011539799.1:p.Ala23Ser
XM_011541500.3:c.49G>T XP_011539802.1:p.Ala17Ser
XM_011541501.2:c.49G>T XP_011539803.1:p.Ala17Ser
XM_011541502.2:c.49G>T XP_011539804.1:p.Ala17Ser
XM_011541503.2:c.91G>T XP_011539805.1:p.Ala31Ser
XM_011541504.2:c.49G>T XP_011539806.1:p.Ala17Ser
XM_011541505.2:c.-25G>T XP_011539807.1:n.-25G>T
XM_011541506.2:c.-25G>T XP_011539808.1:n.-25G>T
XM_017001331.1:c.49G>T XP_016856820.1:p.Ala17Ser
XM_017001332.1:c.49G>T XP_016856821.1:p.Ala17Ser
XM_017001333.1:c.49G>T XP_016856822.1:p.Ala17Ser
XM_017001334.1:c.49G>T XP_016856823.1:p.Ala17Ser
XM_017001335.1:c.-164G>T XP_016856824.1:n.-164G>T
XM_017001336.1:c.-256G>T XP_016856825.1:n.-256G>T
XM_017001337.1:c.-256G>T XP_016856826.1:n.-256G>T
XM_024447244.1:c.-265G>T XP_024303012.1:n.-265G>T
XM_024447245.1:c.-226G>T XP_024303013.1:n.-226G>T
XM_024447248.1:c.-223G>T XP_024303016.1:n.-223G>T
XM_024447249.1:c.-719G>T XP_024303017.1:n.-719G>T
XM_024447250.1:c.-722G>T XP_024303018.1:n.-722G>T
XM_024447251.1:c.-413G>T XP_024303019.1:n.-413G>T
XR_001737190.1:n.158G>T
XR_001737192.1:n.86G>T
XR_002956643.1:n.266G>T
XR_002956644.1:n.284G>T
XR_946658.2:n.152G>T
NM_001048171.2:c.49G>T NP_001041636.2:p.Ala17Ser
NM_001128425.2:c.91G>T MANE Plus Clinical NP_001121897.1:p.Ala31Ser
NM_001048172.2:c.49G>T NP_001041637.1:p.Ala17Ser
NM_001048173.2:c.49G>T NP_001041638.1:p.Ala17Ser
NM_001048174.2:c.49G>T MANE Select NP_001041639.1:p.Ala17Ser
NM_001293190.2:c.91G>T NP_001280119.1:p.Ala31Ser
NM_001293191.2:c.49G>T NP_001280120.1:p.Ala17Ser
NM_001293192.2:c.-164G>T NP_001280121.1:n.-164G>T
NM_001293195.2:c.49G>T NP_001280124.1:p.Ala17Ser
NM_001293196.2:c.-164G>T NP_001280125.1:n.-164G>T
NM_001350650.2:c.-223G>T NP_001337579.1:n.-223G>T
NM_001350651.2:c.-159G>T NP_001337580.1:n.-159G>T
NM_012222.3:c.91G>T NP_036354.1:p.Ala31Ser
NR_146882.2:n.277G>T
NR_146883.2:n.200G>T