Canonical Allele Identifier: CA417879938
Gene: MUTYH HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45797865C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332193C>T , CM000663.2:g.45332193C>T GRCh38
NC_000001.10:g.45797865C>T , CM000663.1:g.45797865C>T GRCh37
NC_000001.9:g.45570452C>T NCBI36
NG_008189.1:g.13278G>A , LRG_220:g.13278G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.438G>A ENSP00000410263.2:p.Val146=
ENST00000435155.2:c.855G>A ENSP00000403655.2:p.Val285=
ENST00000467459.6:c.822G>A ENSP00000435889.2:p.Val274=
ENST00000483127.2:c.840G>A ENSP00000436469.2:p.Val280=
ENST00000485271.6:c.822G>A ENSP00000431264.2:p.Val274=
ENST00000529892.6:c.864G>A ENSP00000432528.2:p.Val288=
ENST00000533178.6:c.*151G>A ENSP00000436430.2:n.*151G>A
ENST00000672314.2:c.822G>A ENSP00000500828.2:p.Val274=
ENST00000710952.2:c.906G>A MANE Plus Clinical ENSP00000518552.2:p.Val302=
ENST00000672818.3:c.897G>A ENSP00000500891.1:p.Val299=
ENST00000456914.7:c.822G>A MANE Select ENSP00000407590.2:p.Val274=
ENST00000461495.6:c.*561G>A ENSP00000437166.1:n.*561G>A
ENST00000671898.1:c.1410G>A ENSP00000499896.1:p.Val470=
ENST00000672011.1:c.*151G>A ENSP00000500418.1:n.*151G>A
ENST00000672314.1:c.822G>A ENSP00000500828.1:p.Val274=
ENST00000672593.1:c.*875G>A ENSP00000500455.1:n.*875G>A
ENST00000672764.1:c.*151G>A ENSP00000500886.1:n.*151G>A
ENST00000672818.2:c.897G>A ENSP00000500891.1:p.Val299=
ENST00000673134.1:c.*519G>A ENSP00000500526.1:n.*519G>A
ENST00000354383.10:c.825G>A ENSP00000346354.6:p.Val275=
ENST00000355498.6:c.822G>A ENSP00000347685.2:p.Val274=
ENST00000372098.7:c.897G>A ENSP00000361170.3:p.Val299=
ENST00000372104.5:c.822G>A ENSP00000361176.1:p.Val274=
ENST00000372110.7:c.867G>A ENSP00000361182.3:p.Val289=
ENST00000372115.7:c.864G>A ENSP00000361187.3:p.Val288=
ENST00000412971.5:c.438G>A ENSP00000410263.1:p.Val146=
ENST00000435155.1:c.855G>A ENSP00000403655.1:p.Val285=
ENST00000448481.5:c.855G>A ENSP00000409718.1:p.Val285=
ENST00000450313.5:c.906G>A ENSP00000408176.1:p.Val302=
ENST00000456914.6:c.822G>A ENSP00000407590.2:p.Val274=
ENST00000461495.5:c.*561G>A ENSP00000437166.1:n.*561G>A
ENST00000462388.5:n.513G>A
ENST00000466231.1:n.187G>A
ENST00000467459.5:c.216G>A ENSP00000435889.1:p.Val72=
ENST00000470256.5:c.*151G>A ENSP00000434985.1:n.*151G>A
ENST00000475516.5:c.*635G>A ENSP00000433843.1:n.*635G>A
ENST00000481571.5:c.*635G>A ENSP00000436597.1:n.*635G>A
ENST00000488731.6:c.187+570G>A ENSP00000432330.1:n.187+570G>A
ENST00000528013.6:c.864G>A ENSP00000433130.2:p.Val288=
ENST00000529892.5:c.86G>A
ENST00000529984.5:c.187+570G>A ENSP00000437093.1:n.187+570G>A
ENST00000531105.5:c.115+2198G>A ENSP00000431292.1:n.115+2198G>A
ENST00000533178.5:c.451G>A ENSP00000436430.1:n.451G>A
NM_001048171.1:c.864G>A NP_001041636.1:p.Val288=
NM_001048172.1:c.825G>A NP_001041637.1:p.Val275=
NM_001048173.1:c.822G>A NP_001041638.1:p.Val274=
NM_001048174.1:c.822G>A NP_001041639.1:p.Val274=
NM_001128425.1:c.906G>A , LRG_220t1:c.906G>A NP_001121897.1:p.Val302=
NM_001293190.1:c.867G>A NP_001280119.1:p.Val289=
NM_001293191.1:c.855G>A NP_001280120.1:p.Val285=
NM_001293192.1:c.546G>A NP_001280121.1:p.Val182=
NM_001293195.1:c.822G>A NP_001280124.1:p.Val274=
NM_001293196.1:c.546G>A NP_001280125.1:p.Val182=
NM_012222.2:c.897G>A NP_036354.1:p.Val299=
XM_011541497.1:c.882G>A XP_011539799.1:p.Val294=
XM_011541498.1:c.864G>A XP_011539800.1:p.Val288=
XM_011541499.1:c.864G>A XP_011539801.1:p.Val288=
XM_011541500.1:c.864G>A XP_011539802.1:p.Val288=
XM_011541501.1:c.864G>A XP_011539803.1:p.Val288=
XM_011541502.1:c.864G>A XP_011539804.1:p.Val288=
XM_011541503.1:c.864G>A XP_011539805.1:p.Val288=
XM_011541504.1:c.855G>A XP_011539806.1:p.Val285=
XM_011541505.1:c.444G>A XP_011539807.1:p.Val148=
XM_011541506.1:c.444G>A XP_011539808.1:p.Val148=
XM_011541507.1:c.435G>A XP_011539809.1:p.Val145=
XM_011541508.1:c.450G>A XP_011539810.1:p.Val150=
XR_946658.1:n.953G>A
NM_001350650.1:c.477G>A NP_001337579.1:p.Val159=
NM_001350651.1:c.477G>A NP_001337580.1:p.Val159=
NR_146882.1:n.1080G>A
NR_146883.1:n.894G>A
XM_011541497.3:c.882G>A XP_011539799.1:p.Val294=
XM_011541500.3:c.864G>A XP_011539802.1:p.Val288=
XM_011541501.2:c.864G>A XP_011539803.1:p.Val288=
XM_011541502.2:c.864G>A XP_011539804.1:p.Val288=
XM_011541503.2:c.864G>A XP_011539805.1:p.Val288=
XM_011541504.2:c.855G>A XP_011539806.1:p.Val285=
XM_011541505.2:c.444G>A XP_011539807.1:p.Val148=
XM_011541506.2:c.444G>A XP_011539808.1:p.Val148=
XM_017001331.1:c.864G>A XP_016856820.1:p.Val288=
XM_017001332.1:c.864G>A XP_016856821.1:p.Val288=
XM_017001333.1:c.864G>A XP_016856822.1:p.Val288=
XM_017001334.1:c.825G>A XP_016856823.1:p.Val275=
XM_017001335.1:c.546G>A XP_016856824.1:p.Val182=
XM_017001336.1:c.477G>A XP_016856825.1:p.Val159=
XM_017001337.1:c.477G>A XP_016856826.1:p.Val159=
XM_024447244.1:c.477G>A XP_024303012.1:p.Val159=
XM_024447245.1:c.477G>A XP_024303013.1:p.Val159=
XM_024447248.1:c.435G>A XP_024303016.1:p.Val145=
XM_024447249.1:c.306G>A XP_024303017.1:p.Val102=
XM_024447250.1:c.306G>A XP_024303018.1:p.Val102=
XM_024447251.1:c.306G>A XP_024303019.1:p.Val102=
XR_001737190.1:n.867G>A
XR_001737192.1:n.679G>A
XR_002956643.1:n.859G>A
XR_002956644.1:n.1394G>A
XR_946658.2:n.967G>A
NM_001048171.2:c.822G>A NP_001041636.2:p.Val274=
NM_001128425.2:c.906G>A MANE Plus Clinical NP_001121897.1:p.Val302=
NM_001048172.2:c.825G>A NP_001041637.1:p.Val275=
NM_001048173.2:c.822G>A NP_001041638.1:p.Val274=
NM_001048174.2:c.822G>A MANE Select NP_001041639.1:p.Val274=
NM_001293190.2:c.867G>A NP_001280119.1:p.Val289=
NM_001293191.2:c.855G>A NP_001280120.1:p.Val285=
NM_001293192.2:c.546G>A NP_001280121.1:p.Val182=
NM_001293195.2:c.822G>A NP_001280124.1:p.Val274=
NM_001293196.2:c.546G>A NP_001280125.1:p.Val182=
NM_001350650.2:c.477G>A NP_001337579.1:p.Val159=
NM_001350651.2:c.477G>A NP_001337580.1:p.Val159=
NM_012222.3:c.897G>A NP_036354.1:p.Val299=
NR_146882.2:n.1050G>A
NR_146883.2:n.899G>A