Canonical Allele Identifier: CA340132720

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45796964A>C (hg19) ; chr1:g.45331292A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331292A>C , CM000663.2:g.45331292A>C	GRCh38
NC_000001.10:g.45796964A>C , CM000663.1:g.45796964A>C	GRCh37
NC_000001.9:g.45569551A>C	NCBI36
NG_008189.1:g.14179T>G , LRG_220:g.14179T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.898T>G	ENSP00000410263.2:p.Tyr300Asp
ENST00000435155.2:c.1315T>G	ENSP00000403655.2:p.Tyr439Asp
ENST00000467459.6:c.*144T>G	ENSP00000435889.2:n.*144T>G
ENST00000483127.2:c.1300T>G	ENSP00000436469.2:p.Tyr434Asp
ENST00000485271.6:c.1282T>G	ENSP00000431264.2:p.Tyr428Asp
ENST00000529892.6:c.1135T>G	ENSP00000432528.2:p.Tyr379Asp
ENST00000533178.6:c.*611T>G	ENSP00000436430.2:n.*611T>G
ENST00000672314.2:c.1282T>G	ENSP00000500828.2:p.Tyr428Asp
ENST00000710952.2:c.1366T>G MANE Plus Clinical	ENSP00000518552.2:p.Tyr456Asp
ENST00000672818.3:c.1357T>G	ENSP00000500891.1:p.Tyr453Asp
ENST00000456914.7:c.1282T>G MANE Select	ENSP00000407590.2:p.Tyr428Asp
ENST00000671898.1:c.1870T>G	ENSP00000499896.1:p.Tyr624Asp
ENST00000672011.1:c.*611T>G	ENSP00000500418.1:n.*611T>G
ENST00000672314.1:c.1282T>G	ENSP00000500828.1:p.Tyr428Asp
ENST00000672818.2:c.1357T>G	ENSP00000500891.1:p.Tyr453Asp
ENST00000673134.1:c.*979T>G	ENSP00000500526.1:n.*979T>G
ENST00000354383.10:c.1285T>G	ENSP00000346354.6:p.Tyr429Asp
ENST00000355498.6:c.1282T>G	ENSP00000347685.2:p.Tyr428Asp
ENST00000372098.7:c.1357T>G	ENSP00000361170.3:p.Tyr453Asp
ENST00000372104.5:c.1282T>G	ENSP00000361176.1:p.Tyr428Asp
ENST00000372110.7:c.1327T>G	ENSP00000361182.3:p.Tyr443Asp
ENST00000372115.7:c.1324T>G	ENSP00000361187.3:p.Tyr442Asp
ENST00000448481.5:c.1315T>G	ENSP00000409718.1:p.Tyr439Asp
ENST00000450313.5:c.1366T>G	ENSP00000408176.1:p.Tyr456Asp
ENST00000456914.6:c.1282T>G	ENSP00000407590.2:p.Tyr428Asp
ENST00000467459.5:c.699T>G	ENSP00000435889.1:n.699T>G
ENST00000475516.5:c.*1095T>G	ENSP00000433843.1:n.*1095T>G
ENST00000481571.5:c.*1095T>G	ENSP00000436597.1:n.*1095T>G
ENST00000482094.5:n.603T>G
ENST00000488731.6:c.367T>G	ENSP00000432330.1:p.Tyr123Asp
ENST00000528013.6:c.1324T>G	ENSP00000433130.2:p.Tyr442Asp
ENST00000529892.5:c.357T>G
ENST00000529984.5:c.367T>G	ENSP00000437093.1:p.Tyr123Asp
ENST00000531105.5:c.116-1855T>G	ENSP00000431292.1:n.116-1855T>G
ENST00000533178.5:c.911T>G	ENSP00000436430.1:n.911T>G
NM_001048171.1:c.1324T>G	NP_001041636.1:p.Tyr442Asp
NM_001048172.1:c.1285T>G	NP_001041637.1:p.Tyr429Asp
NM_001048173.1:c.1282T>G	NP_001041638.1:p.Tyr428Asp
NM_001048174.1:c.1282T>G	NP_001041639.1:p.Tyr428Asp
NM_001128425.1:c.1366T>G , LRG_220t1:c.1366T>G	NP_001121897.1:p.Tyr456Asp
NM_001293190.1:c.1327T>G	NP_001280119.1:p.Tyr443Asp
NM_001293191.1:c.1315T>G	NP_001280120.1:p.Tyr439Asp
NM_001293192.1:c.1006T>G	NP_001280121.1:p.Tyr336Asp
NM_001293195.1:c.1282T>G	NP_001280124.1:p.Tyr428Asp
NM_001293196.1:c.1006T>G	NP_001280125.1:p.Tyr336Asp
NM_012222.2:c.1357T>G	NP_036354.1:p.Tyr453Asp
XM_011541497.1:c.1342T>G	XP_011539799.1:p.Tyr448Asp
XM_011541498.1:c.1324T>G	XP_011539800.1:p.Tyr442Asp
XM_011541499.1:c.1324T>G	XP_011539801.1:p.Tyr442Asp
XM_011541500.1:c.1324T>G	XP_011539802.1:p.Tyr442Asp
XM_011541501.1:c.1324T>G	XP_011539803.1:p.Tyr442Asp
XM_011541502.1:c.1324T>G	XP_011539804.1:p.Tyr442Asp
XM_011541503.1:c.1324T>G	XP_011539805.1:p.Tyr442Asp
XM_011541504.1:c.1315T>G	XP_011539806.1:p.Tyr439Asp
XM_011541505.1:c.904T>G	XP_011539807.1:p.Tyr302Asp
XM_011541506.1:c.904T>G	XP_011539808.1:p.Tyr302Asp
XM_011541507.1:c.895T>G	XP_011539809.1:p.Tyr299Asp
XM_011541508.1:c.910T>G	XP_011539810.1:p.Tyr304Asp
XR_946658.1:n.1413T>G
NM_001350650.1:c.937T>G	NP_001337579.1:p.Tyr313Asp
NM_001350651.1:c.937T>G	NP_001337580.1:p.Tyr313Asp
NR_146882.1:n.1540T>G
NR_146883.1:n.1354T>G
XM_011541497.3:c.1342T>G	XP_011539799.1:p.Tyr448Asp
XM_011541500.3:c.1324T>G	XP_011539802.1:p.Tyr442Asp
XM_011541501.2:c.1324T>G	XP_011539803.1:p.Tyr442Asp
XM_011541502.2:c.1324T>G	XP_011539804.1:p.Tyr442Asp
XM_011541503.2:c.1324T>G	XP_011539805.1:p.Tyr442Asp
XM_011541504.2:c.1315T>G	XP_011539806.1:p.Tyr439Asp
XM_011541505.2:c.904T>G	XP_011539807.1:p.Tyr302Asp
XM_011541506.2:c.904T>G	XP_011539808.1:p.Tyr302Asp
XM_017001331.1:c.1324T>G	XP_016856820.1:p.Tyr442Asp
XM_017001332.1:c.1324T>G	XP_016856821.1:p.Tyr442Asp
XM_017001333.1:c.1324T>G	XP_016856822.1:p.Tyr442Asp
XM_017001334.1:c.1285T>G	XP_016856823.1:p.Tyr429Asp
XM_017001335.1:c.1006T>G	XP_016856824.1:p.Tyr336Asp
XM_017001336.1:c.937T>G	XP_016856825.1:p.Tyr313Asp
XM_017001337.1:c.937T>G	XP_016856826.1:p.Tyr313Asp
XM_024447244.1:c.937T>G	XP_024303012.1:p.Tyr313Asp
XM_024447245.1:c.937T>G	XP_024303013.1:p.Tyr313Asp
XM_024447248.1:c.895T>G	XP_024303016.1:p.Tyr299Asp
XM_024447249.1:c.766T>G	XP_024303017.1:p.Tyr256Asp
XM_024447250.1:c.766T>G	XP_024303018.1:p.Tyr256Asp
XM_024447251.1:c.766T>G	XP_024303019.1:p.Tyr256Asp
XR_001737190.1:n.1327T>G
XR_001737192.1:n.1139T>G
XR_002956643.1:n.1319T>G
XR_002956644.1:n.1854T>G
XR_946658.2:n.1427T>G
NM_001048171.2:c.1282T>G	NP_001041636.2:p.Tyr428Asp
NM_001128425.2:c.1366T>G MANE Plus Clinical	NP_001121897.1:p.Tyr456Asp
NM_001048172.2:c.1285T>G	NP_001041637.1:p.Tyr429Asp
NM_001048173.2:c.1282T>G	NP_001041638.1:p.Tyr428Asp
NM_001048174.2:c.1282T>G MANE Select	NP_001041639.1:p.Tyr428Asp
NM_001293190.2:c.1327T>G	NP_001280119.1:p.Tyr443Asp
NM_001293191.2:c.1315T>G	NP_001280120.1:p.Tyr439Asp
NM_001293192.2:c.1006T>G	NP_001280121.1:p.Tyr336Asp
NM_001293195.2:c.1282T>G	NP_001280124.1:p.Tyr428Asp
NM_001293196.2:c.1006T>G	NP_001280125.1:p.Tyr336Asp
NM_001350650.2:c.937T>G	NP_001337579.1:p.Tyr313Asp
NM_001350651.2:c.937T>G	NP_001337580.1:p.Tyr313Asp
NM_012222.3:c.1357T>G	NP_036354.1:p.Tyr453Asp
NR_146882.2:n.1510T>G
NR_146883.2:n.1359T>G