Canonical Allele Identifier: CA340132630
Gene: MUTYH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331247G>A , CM000663.2:g.45331247G>A GRCh38
NC_000001.10:g.45796919G>A , CM000663.1:g.45796919G>A GRCh37
NC_000001.9:g.45569506G>A NCBI36
NG_008189.1:g.14224C>T , LRG_220:g.14224C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000672818.3:c.1402C>T ENSP00000500891.1:p.Pro468Ser
ENST00000456914.7:c.1327C>T MANE Select ENSP00000407590.2:p.Pro443Ser
ENST00000671898.1:c.1915C>T ENSP00000499896.1:p.Pro639Ser
ENST00000672011.1:c.*656C>T ENSP00000500418.1:n.*656C>T
ENST00000672314.1:c.1327C>T ENSP00000500828.1:p.Pro443Ser
ENST00000672818.2:c.1402C>T ENSP00000500891.1:p.Pro468Ser
ENST00000673134.1:c.*1024C>T ENSP00000500526.1:n.*1024C>T
ENST00000354383.10:c.1330C>T ENSP00000346354.6:p.Pro444Ser
ENST00000355498.6:c.1327C>T ENSP00000347685.2:p.Pro443Ser
ENST00000372098.7:c.1402C>T ENSP00000361170.3:p.Pro468Ser
ENST00000372104.5:c.1327C>T ENSP00000361176.1:p.Pro443Ser
ENST00000372110.7:c.1372C>T ENSP00000361182.3:p.Pro458Ser
ENST00000372115.7:c.1369C>T ENSP00000361187.3:p.Pro457Ser
ENST00000448481.5:c.1360C>T ENSP00000409718.1:p.Pro454Ser
ENST00000450313.5:c.1411C>T ENSP00000408176.1:p.Pro471Ser
ENST00000456914.6:c.1327C>T ENSP00000407590.2:p.Pro443Ser
ENST00000467459.5:n.744C>T ENSP00000435889.1:n.744C>T
ENST00000475516.5:c.*1140C>T ENSP00000433843.1:n.*1140C>T
ENST00000481571.5:c.*1140C>T ENSP00000436597.1:n.*1140C>T
ENST00000482094.5:n.648C>T
ENST00000485271.5:n.24C>T
ENST00000488731.6:c.412C>T ENSP00000432330.1:p.Pro138Ser
ENST00000528013.6:c.1369C>T ENSP00000433130.2:p.Pro457Ser
ENST00000529892.5:n.402C>T
ENST00000529984.5:c.412C>T ENSP00000437093.1:p.Pro138Ser
ENST00000531105.5:c.116-1810C>T ENSP00000431292.1:n.116-1810C>T
ENST00000533178.5:n.956C>T ENSP00000436430.1:n.956C>T
NM_001048171.1:c.1369C>T NP_001041636.1:p.Pro457Ser
NM_001048172.1:c.1330C>T NP_001041637.1:p.Pro444Ser
NM_001048173.1:c.1327C>T NP_001041638.1:p.Pro443Ser
NM_001048174.1:c.1327C>T NP_001041639.1:p.Pro443Ser
NM_001128425.1:c.1411C>T , LRG_220t1:c.1411C>T NP_001121897.1:p.Pro471Ser
NM_001293190.1:c.1372C>T NP_001280119.1:p.Pro458Ser
NM_001293191.1:c.1360C>T NP_001280120.1:p.Pro454Ser
NM_001293192.1:c.1051C>T NP_001280121.1:p.Pro351Ser
NM_001293195.1:c.1327C>T NP_001280124.1:p.Pro443Ser
NM_001293196.1:c.1051C>T NP_001280125.1:p.Pro351Ser
NM_012222.2:c.1402C>T NP_036354.1:p.Pro468Ser
XM_011541497.1:c.1387C>T XP_011539799.1:p.Pro463Ser
XM_011541498.1:c.1369C>T XP_011539800.1:p.Pro457Ser
XM_011541499.1:c.1369C>T XP_011539801.1:p.Pro457Ser
XM_011541500.1:c.1369C>T XP_011539802.1:p.Pro457Ser
XM_011541501.1:c.1369C>T XP_011539803.1:p.Pro457Ser
XM_011541502.1:c.1369C>T XP_011539804.1:p.Pro457Ser
XM_011541503.1:c.1369C>T XP_011539805.1:p.Pro457Ser
XM_011541504.1:c.1360C>T XP_011539806.1:p.Pro454Ser
XM_011541505.1:c.949C>T XP_011539807.1:p.Pro317Ser
XM_011541506.1:c.949C>T XP_011539808.1:p.Pro317Ser
XM_011541507.1:c.940C>T XP_011539809.1:p.Pro314Ser
XM_011541508.1:c.955C>T XP_011539810.1:p.Pro319Ser
XR_946658.1:n.1458C>T
NM_001350650.1:c.982C>T NP_001337579.1:p.Pro328Ser
NM_001350651.1:c.982C>T NP_001337580.1:p.Pro328Ser
NR_146882.1:n.1585C>T
NR_146883.1:n.1399C>T
XM_011541497.3:c.1387C>T XP_011539799.1:p.Pro463Ser
XM_011541500.3:c.1369C>T XP_011539802.1:p.Pro457Ser
XM_011541501.2:c.1369C>T XP_011539803.1:p.Pro457Ser
XM_011541502.2:c.1369C>T XP_011539804.1:p.Pro457Ser
XM_011541503.2:c.1369C>T XP_011539805.1:p.Pro457Ser
XM_011541504.2:c.1360C>T XP_011539806.1:p.Pro454Ser
XM_011541505.2:c.949C>T XP_011539807.1:p.Pro317Ser
XM_011541506.2:c.949C>T XP_011539808.1:p.Pro317Ser
XM_017001331.1:c.1369C>T XP_016856820.1:p.Pro457Ser
XM_017001332.1:c.1369C>T XP_016856821.1:p.Pro457Ser
XM_017001333.1:c.1369C>T XP_016856822.1:p.Pro457Ser
XM_017001334.1:c.1330C>T XP_016856823.1:p.Pro444Ser
XM_017001335.1:c.1051C>T XP_016856824.1:p.Pro351Ser
XM_017001336.1:c.982C>T XP_016856825.1:p.Pro328Ser
XM_017001337.1:c.982C>T XP_016856826.1:p.Pro328Ser
XM_024447244.1:c.982C>T XP_024303012.1:p.Pro328Ser
XM_024447245.1:c.982C>T XP_024303013.1:p.Pro328Ser
XM_024447248.1:c.940C>T XP_024303016.1:p.Pro314Ser
XM_024447249.1:c.811C>T XP_024303017.1:p.Pro271Ser
XM_024447250.1:c.811C>T XP_024303018.1:p.Pro271Ser
XM_024447251.1:c.811C>T XP_024303019.1:p.Pro271Ser
XR_001737190.1:n.1372C>T
XR_001737192.1:n.1184C>T
XR_002956643.1:n.1364C>T
XR_002956644.1:n.1899C>T
XR_946658.2:n.1472C>T
NM_001048171.2:c.1327C>T NP_001041636.2:p.Pro443Ser
NM_001128425.2:c.1411C>T NP_001121897.1:p.Pro471Ser
NM_001048172.2:c.1330C>T NP_001041637.1:p.Pro444Ser
NM_001048173.2:c.1327C>T NP_001041638.1:p.Pro443Ser
NM_001048174.2:c.1327C>T MANE Select NP_001041639.1:p.Pro443Ser
NM_001293190.2:c.1372C>T NP_001280119.1:p.Pro458Ser
NM_001293191.2:c.1360C>T NP_001280120.1:p.Pro454Ser
NM_001293192.2:c.1051C>T NP_001280121.1:p.Pro351Ser
NM_001293195.2:c.1327C>T NP_001280124.1:p.Pro443Ser
NM_001293196.2:c.1051C>T NP_001280125.1:p.Pro351Ser
NM_001350650.2:c.982C>T NP_001337579.1:p.Pro328Ser
NM_001350651.2:c.982C>T NP_001337580.1:p.Pro328Ser
NM_012222.3:c.1402C>T NP_036354.1:p.Pro468Ser
NR_146882.2:n.1555C>T
NR_146883.2:n.1404C>T