Canonical Allele Identifier: CA340132621

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 2453352
• ClinVar RCV Id: RCV003182807
• dbSNP Id: rs192816572
• MyVariant Identifiers: chr1:g.45796913C>A (hg19) ; chr1:g.45331241C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331241C>A , CM000663.2:g.45331241C>A	GRCh38
NC_000001.10:g.45796913C>A , CM000663.1:g.45796913C>A	GRCh37
NC_000001.9:g.45569500C>A	NCBI36
NG_008189.1:g.14230G>T , LRG_220:g.14230G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.949G>T	ENSP00000410263.2:p.Ala317Ser
ENST00000435155.2:c.1366G>T	ENSP00000403655.2:p.Ala456Ser
ENST00000467459.6:c.*195G>T	ENSP00000435889.2:n.*195G>T
ENST00000483127.2:c.1351G>T	ENSP00000436469.2:p.Ala451Ser
ENST00000485271.6:c.1333G>T	ENSP00000431264.2:p.Ala445Ser
ENST00000529892.6:c.1186G>T	ENSP00000432528.2:p.Ala396Ser
ENST00000533178.6:c.*662G>T	ENSP00000436430.2:n.*662G>T
ENST00000672314.2:c.1333G>T	ENSP00000500828.2:p.Ala445Ser
ENST00000710952.2:c.1417G>T MANE Plus Clinical	ENSP00000518552.2:p.Ala473Ser
ENST00000672818.3:c.1408G>T	ENSP00000500891.1:p.Ala470Ser
ENST00000456914.7:c.1333G>T MANE Select	ENSP00000407590.2:p.Ala445Ser
ENST00000671898.1:c.1921G>T	ENSP00000499896.1:p.Ala641Ser
ENST00000672011.1:c.*662G>T	ENSP00000500418.1:n.*662G>T
ENST00000672314.1:c.1333G>T	ENSP00000500828.1:p.Ala445Ser
ENST00000672818.2:c.1408G>T	ENSP00000500891.1:p.Ala470Ser
ENST00000673134.1:c.*1030G>T	ENSP00000500526.1:n.*1030G>T
ENST00000354383.10:c.1336G>T	ENSP00000346354.6:p.Ala446Ser
ENST00000355498.6:c.1333G>T	ENSP00000347685.2:p.Ala445Ser
ENST00000372098.7:c.1408G>T	ENSP00000361170.3:p.Ala470Ser
ENST00000372104.5:c.1333G>T	ENSP00000361176.1:p.Ala445Ser
ENST00000372110.7:c.1378G>T	ENSP00000361182.3:p.Ala460Ser
ENST00000372115.7:c.1375G>T	ENSP00000361187.3:p.Ala459Ser
ENST00000448481.5:c.1366G>T	ENSP00000409718.1:p.Ala456Ser
ENST00000450313.5:c.1417G>T	ENSP00000408176.1:p.Ala473Ser
ENST00000456914.6:c.1333G>T	ENSP00000407590.2:p.Ala445Ser
ENST00000467459.5:c.750G>T	ENSP00000435889.1:n.750G>T
ENST00000475516.5:c.*1146G>T	ENSP00000433843.1:n.*1146G>T
ENST00000481571.5:c.*1146G>T	ENSP00000436597.1:n.*1146G>T
ENST00000482094.5:n.654G>T
ENST00000485271.5:c.30G>T
ENST00000488731.6:c.418G>T	ENSP00000432330.1:p.Ala140Ser
ENST00000528013.6:c.1375G>T	ENSP00000433130.2:p.Ala459Ser
ENST00000529892.5:c.408G>T
ENST00000529984.5:c.418G>T	ENSP00000437093.1:p.Ala140Ser
ENST00000531105.5:c.116-1804G>T	ENSP00000431292.1:n.116-1804G>T
ENST00000533178.5:c.962G>T	ENSP00000436430.1:n.962G>T
NM_001048171.1:c.1375G>T	NP_001041636.1:p.Ala459Ser
NM_001048172.1:c.1336G>T	NP_001041637.1:p.Ala446Ser
NM_001048173.1:c.1333G>T	NP_001041638.1:p.Ala445Ser
NM_001048174.1:c.1333G>T	NP_001041639.1:p.Ala445Ser
NM_001128425.1:c.1417G>T , LRG_220t1:c.1417G>T	NP_001121897.1:p.Ala473Ser
NM_001293190.1:c.1378G>T	NP_001280119.1:p.Ala460Ser
NM_001293191.1:c.1366G>T	NP_001280120.1:p.Ala456Ser
NM_001293192.1:c.1057G>T	NP_001280121.1:p.Ala353Ser
NM_001293195.1:c.1333G>T	NP_001280124.1:p.Ala445Ser
NM_001293196.1:c.1057G>T	NP_001280125.1:p.Ala353Ser
NM_012222.2:c.1408G>T	NP_036354.1:p.Ala470Ser
XM_011541497.1:c.1393G>T	XP_011539799.1:p.Ala465Ser
XM_011541498.1:c.1375G>T	XP_011539800.1:p.Ala459Ser
XM_011541499.1:c.1375G>T	XP_011539801.1:p.Ala459Ser
XM_011541500.1:c.1375G>T	XP_011539802.1:p.Ala459Ser
XM_011541501.1:c.1375G>T	XP_011539803.1:p.Ala459Ser
XM_011541502.1:c.1375G>T	XP_011539804.1:p.Ala459Ser
XM_011541503.1:c.1375G>T	XP_011539805.1:p.Ala459Ser
XM_011541504.1:c.1366G>T	XP_011539806.1:p.Ala456Ser
XM_011541505.1:c.955G>T	XP_011539807.1:p.Ala319Ser
XM_011541506.1:c.955G>T	XP_011539808.1:p.Ala319Ser
XM_011541507.1:c.946G>T	XP_011539809.1:p.Ala316Ser
XM_011541508.1:c.961G>T	XP_011539810.1:p.Ala321Ser
XR_946658.1:n.1464G>T
NM_001350650.1:c.988G>T	NP_001337579.1:p.Ala330Ser
NM_001350651.1:c.988G>T	NP_001337580.1:p.Ala330Ser
NR_146882.1:n.1591G>T
NR_146883.1:n.1405G>T
XM_011541497.3:c.1393G>T	XP_011539799.1:p.Ala465Ser
XM_011541500.3:c.1375G>T	XP_011539802.1:p.Ala459Ser
XM_011541501.2:c.1375G>T	XP_011539803.1:p.Ala459Ser
XM_011541502.2:c.1375G>T	XP_011539804.1:p.Ala459Ser
XM_011541503.2:c.1375G>T	XP_011539805.1:p.Ala459Ser
XM_011541504.2:c.1366G>T	XP_011539806.1:p.Ala456Ser
XM_011541505.2:c.955G>T	XP_011539807.1:p.Ala319Ser
XM_011541506.2:c.955G>T	XP_011539808.1:p.Ala319Ser
XM_017001331.1:c.1375G>T	XP_016856820.1:p.Ala459Ser
XM_017001332.1:c.1375G>T	XP_016856821.1:p.Ala459Ser
XM_017001333.1:c.1375G>T	XP_016856822.1:p.Ala459Ser
XM_017001334.1:c.1336G>T	XP_016856823.1:p.Ala446Ser
XM_017001335.1:c.1057G>T	XP_016856824.1:p.Ala353Ser
XM_017001336.1:c.988G>T	XP_016856825.1:p.Ala330Ser
XM_017001337.1:c.988G>T	XP_016856826.1:p.Ala330Ser
XM_024447244.1:c.988G>T	XP_024303012.1:p.Ala330Ser
XM_024447245.1:c.988G>T	XP_024303013.1:p.Ala330Ser
XM_024447248.1:c.946G>T	XP_024303016.1:p.Ala316Ser
XM_024447249.1:c.817G>T	XP_024303017.1:p.Ala273Ser
XM_024447250.1:c.817G>T	XP_024303018.1:p.Ala273Ser
XM_024447251.1:c.817G>T	XP_024303019.1:p.Ala273Ser
XR_001737190.1:n.1378G>T
XR_001737192.1:n.1190G>T
XR_002956643.1:n.1370G>T
XR_002956644.1:n.1905G>T
XR_946658.2:n.1478G>T
NM_001048171.2:c.1333G>T	NP_001041636.2:p.Ala445Ser
NM_001128425.2:c.1417G>T MANE Plus Clinical	NP_001121897.1:p.Ala473Ser
NM_001048172.2:c.1336G>T	NP_001041637.1:p.Ala446Ser
NM_001048173.2:c.1333G>T	NP_001041638.1:p.Ala445Ser
NM_001048174.2:c.1333G>T MANE Select	NP_001041639.1:p.Ala445Ser
NM_001293190.2:c.1378G>T	NP_001280119.1:p.Ala460Ser
NM_001293191.2:c.1366G>T	NP_001280120.1:p.Ala456Ser
NM_001293192.2:c.1057G>T	NP_001280121.1:p.Ala353Ser
NM_001293195.2:c.1333G>T	NP_001280124.1:p.Ala445Ser
NM_001293196.2:c.1057G>T	NP_001280125.1:p.Ala353Ser
NM_001350650.2:c.988G>T	NP_001337579.1:p.Ala330Ser
NM_001350651.2:c.988G>T	NP_001337580.1:p.Ala330Ser
NM_012222.3:c.1408G>T	NP_036354.1:p.Ala470Ser
NR_146882.2:n.1561G>T
NR_146883.2:n.1410G>T