Canonical Allele Identifier: CA340135238

Gene: MUTYH

Linked Data

• dbSNP Id: rs2149145924
• MyVariant Identifiers: chr1:g.45798156G>A (hg19) ; chr1:g.45332484G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332484G>A , CM000663.2:g.45332484G>A	GRCh38
NC_000001.10:g.45798156G>A , CM000663.1:g.45798156G>A	GRCh37
NC_000001.9:g.45570743G>A	NCBI36
NG_008189.1:g.12987C>T , LRG_220:g.12987C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.227C>T	ENSP00000410263.2:p.Thr76Ile
ENST00000435155.2:c.644C>T	ENSP00000403655.2:p.Thr215Ile
ENST00000467459.6:c.611C>T	ENSP00000435889.2:p.Thr204Ile
ENST00000483127.2:c.629C>T	ENSP00000436469.2:p.Thr210Ile
ENST00000485271.6:c.611C>T	ENSP00000431264.2:p.Thr204Ile
ENST00000529892.6:c.653C>T	ENSP00000432528.2:p.Thr218Ile
ENST00000533178.6:c.234C>T	ENSP00000436430.2:p.Asn78=
ENST00000672314.2:c.611C>T	ENSP00000500828.2:p.Thr204Ile
ENST00000674679.2:c.*523C>T	ENSP00000501623.2:n.*523C>T
ENST00000710952.2:c.695C>T MANE Plus Clinical	ENSP00000518552.2:p.Thr232Ile
ENST00000672818.3:c.686C>T	ENSP00000500891.1:p.Thr229Ile
ENST00000450313.6:c.621C>T	ENSP00000408176.2:p.Asn207=
ENST00000456914.7:c.611C>T MANE Select	ENSP00000407590.2:p.Thr204Ile
ENST00000461495.6:c.*350C>T	ENSP00000437166.1:n.*350C>T
ENST00000671898.1:c.1199C>T	ENSP00000499896.1:p.Thr400Ile
ENST00000672011.1:c.579C>T	ENSP00000500418.1:p.Asn193=
ENST00000672314.1:c.611C>T	ENSP00000500828.1:p.Thr204Ile
ENST00000672593.1:c.*584C>T	ENSP00000500455.1:n.*584C>T
ENST00000672764.1:c.570C>T	ENSP00000500886.1:p.Asn190=
ENST00000672818.2:c.686C>T	ENSP00000500891.1:p.Thr229Ile
ENST00000673134.1:c.*308C>T	ENSP00000500526.1:n.*308C>T
ENST00000674679.1:c.639C>T	ENSP00000501623.1:n.639C>T
ENST00000354383.10:c.614C>T	ENSP00000346354.6:p.Thr205Ile
ENST00000355498.6:c.611C>T	ENSP00000347685.2:p.Thr204Ile
ENST00000372098.7:c.686C>T	ENSP00000361170.3:p.Thr229Ile
ENST00000372104.5:c.611C>T	ENSP00000361176.1:p.Thr204Ile
ENST00000372110.7:c.656C>T	ENSP00000361182.3:p.Thr219Ile
ENST00000372115.7:c.653C>T	ENSP00000361187.3:p.Thr218Ile
ENST00000412971.5:c.227C>T	ENSP00000410263.1:p.Thr76Ile
ENST00000435155.1:c.644C>T	ENSP00000403655.1:p.Thr215Ile
ENST00000448481.5:c.644C>T	ENSP00000409718.1:p.Thr215Ile
ENST00000450313.5:c.695C>T	ENSP00000408176.1:p.Thr232Ile
ENST00000456914.6:c.611C>T	ENSP00000407590.2:p.Thr204Ile
ENST00000461495.5:c.*350C>T	ENSP00000437166.1:n.*350C>T
ENST00000462388.5:n.302C>T
ENST00000467459.5:c.5C>T	ENSP00000435889.1:p.Thr2Ile
ENST00000467940.5:c.*534C>T	ENSP00000436478.1:n.*534C>T
ENST00000470256.5:c.498C>T	ENSP00000434985.1:p.Asn166=
ENST00000475516.5:c.*424C>T	ENSP00000433843.1:n.*424C>T
ENST00000478796.5:n.598C>T
ENST00000481571.5:c.*424C>T	ENSP00000436597.1:n.*424C>T
ENST00000488731.6:c.187+279C>T	ENSP00000432330.1:n.187+279C>T
ENST00000525160.5:c.*262C>T	ENSP00000431568.1:n.*262C>T
ENST00000528013.6:c.653C>T	ENSP00000433130.2:p.Thr218Ile
ENST00000529984.5:c.187+279C>T	ENSP00000437093.1:n.187+279C>T
ENST00000531105.5:c.115+1907C>T	ENSP00000431292.1:n.115+1907C>T
ENST00000533178.5:c.240C>T	ENSP00000436430.1:p.Asn80=
NM_001048171.1:c.653C>T	NP_001041636.1:p.Thr218Ile
NM_001048172.1:c.614C>T	NP_001041637.1:p.Thr205Ile
NM_001048173.1:c.611C>T	NP_001041638.1:p.Thr204Ile
NM_001048174.1:c.611C>T	NP_001041639.1:p.Thr204Ile
NM_001128425.1:c.695C>T , LRG_220t1:c.695C>T	NP_001121897.1:p.Thr232Ile
NM_001293190.1:c.656C>T	NP_001280119.1:p.Thr219Ile
NM_001293191.1:c.644C>T	NP_001280120.1:p.Thr215Ile
NM_001293192.1:c.335C>T	NP_001280121.1:p.Thr112Ile
NM_001293195.1:c.611C>T	NP_001280124.1:p.Thr204Ile
NM_001293196.1:c.335C>T	NP_001280125.1:p.Thr112Ile
NM_012222.2:c.686C>T	NP_036354.1:p.Thr229Ile
XM_011541497.1:c.671C>T	XP_011539799.1:p.Thr224Ile
XM_011541498.1:c.653C>T	XP_011539800.1:p.Thr218Ile
XM_011541499.1:c.653C>T	XP_011539801.1:p.Thr218Ile
XM_011541500.1:c.653C>T	XP_011539802.1:p.Thr218Ile
XM_011541501.1:c.653C>T	XP_011539803.1:p.Thr218Ile
XM_011541502.1:c.653C>T	XP_011539804.1:p.Thr218Ile
XM_011541503.1:c.653C>T	XP_011539805.1:p.Thr218Ile
XM_011541504.1:c.644C>T	XP_011539806.1:p.Thr215Ile
XM_011541505.1:c.233C>T	XP_011539807.1:p.Thr78Ile
XM_011541506.1:c.233C>T	XP_011539808.1:p.Thr78Ile
XM_011541507.1:c.224C>T	XP_011539809.1:p.Thr75Ile
XM_011541508.1:c.239C>T	XP_011539810.1:p.Thr80Ile
XR_946658.1:n.742C>T
NM_001350650.1:c.266C>T	NP_001337579.1:p.Thr89Ile
NM_001350651.1:c.266C>T	NP_001337580.1:p.Thr89Ile
NR_146882.1:n.869C>T
NR_146883.1:n.683C>T
XM_011541497.3:c.671C>T	XP_011539799.1:p.Thr224Ile
XM_011541500.3:c.653C>T	XP_011539802.1:p.Thr218Ile
XM_011541501.2:c.653C>T	XP_011539803.1:p.Thr218Ile
XM_011541502.2:c.653C>T	XP_011539804.1:p.Thr218Ile
XM_011541503.2:c.653C>T	XP_011539805.1:p.Thr218Ile
XM_011541504.2:c.644C>T	XP_011539806.1:p.Thr215Ile
XM_011541505.2:c.233C>T	XP_011539807.1:p.Thr78Ile
XM_011541506.2:c.233C>T	XP_011539808.1:p.Thr78Ile
XM_017001331.1:c.653C>T	XP_016856820.1:p.Thr218Ile
XM_017001332.1:c.653C>T	XP_016856821.1:p.Thr218Ile
XM_017001333.1:c.653C>T	XP_016856822.1:p.Thr218Ile
XM_017001334.1:c.614C>T	XP_016856823.1:p.Thr205Ile
XM_017001335.1:c.335C>T	XP_016856824.1:p.Thr112Ile
XM_017001336.1:c.266C>T	XP_016856825.1:p.Thr89Ile
XM_017001337.1:c.266C>T	XP_016856826.1:p.Thr89Ile
XM_024447244.1:c.266C>T	XP_024303012.1:p.Thr89Ile
XM_024447245.1:c.266C>T	XP_024303013.1:p.Thr89Ile
XM_024447248.1:c.224C>T	XP_024303016.1:p.Thr75Ile
XM_024447249.1:c.95C>T	XP_024303017.1:p.Thr32Ile
XM_024447250.1:c.95C>T	XP_024303018.1:p.Thr32Ile
XM_024447251.1:c.95C>T	XP_024303019.1:p.Thr32Ile
XR_001737190.1:n.656C>T
XR_001737192.1:n.468C>T
XR_002956643.1:n.648C>T
XR_002956644.1:n.1183C>T
XR_946658.2:n.756C>T
NM_001048171.2:c.611C>T	NP_001041636.2:p.Thr204Ile
NM_001128425.2:c.695C>T MANE Plus Clinical	NP_001121897.1:p.Thr232Ile
NM_001048172.2:c.614C>T	NP_001041637.1:p.Thr205Ile
NM_001048173.2:c.611C>T	NP_001041638.1:p.Thr204Ile
NM_001048174.2:c.611C>T MANE Select	NP_001041639.1:p.Thr204Ile
NM_001293190.2:c.656C>T	NP_001280119.1:p.Thr219Ile
NM_001293191.2:c.644C>T	NP_001280120.1:p.Thr215Ile
NM_001293192.2:c.335C>T	NP_001280121.1:p.Thr112Ile
NM_001293195.2:c.611C>T	NP_001280124.1:p.Thr204Ile
NM_001293196.2:c.335C>T	NP_001280125.1:p.Thr112Ile
NM_001350650.2:c.266C>T	NP_001337579.1:p.Thr89Ile
NM_001350651.2:c.266C>T	NP_001337580.1:p.Thr89Ile
NM_012222.3:c.686C>T	NP_036354.1:p.Thr229Ile
NR_146882.2:n.839C>T
NR_146883.2:n.688C>T