Canonical Allele Identifier: CA340133045

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45797189C>A (hg19) ; chr1:g.45331517C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331517C>A , CM000663.2:g.45331517C>A	GRCh38
NC_000001.10:g.45797189C>A , CM000663.1:g.45797189C>A	GRCh37
NC_000001.9:g.45569776C>A	NCBI36
NG_008189.1:g.13954G>T , LRG_220:g.13954G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.758G>T	ENSP00000410263.2:p.Trp253Leu
ENST00000435155.2:c.1175G>T	ENSP00000403655.2:p.Trp392Leu
ENST00000467459.6:c.*4G>T	ENSP00000435889.2:n.*4G>T
ENST00000483127.2:c.1160G>T	ENSP00000436469.2:p.Trp387Leu
ENST00000485271.6:c.1142G>T	ENSP00000431264.2:p.Trp381Leu
ENST00000529892.6:c.995G>T	ENSP00000432528.2:p.Trp332Leu
ENST00000533178.6:c.*471G>T	ENSP00000436430.2:n.*471G>T
ENST00000672314.2:c.1142G>T	ENSP00000500828.2:p.Trp381Leu
ENST00000710952.2:c.1226G>T MANE Plus Clinical	ENSP00000518552.2:p.Trp409Leu
ENST00000672818.3:c.1217G>T	ENSP00000500891.1:p.Trp406Leu
ENST00000456914.7:c.1142G>T MANE Select	ENSP00000407590.2:p.Trp381Leu
ENST00000671898.1:c.1730G>T	ENSP00000499896.1:p.Trp577Leu
ENST00000672011.1:c.*471G>T	ENSP00000500418.1:n.*471G>T
ENST00000672314.1:c.1142G>T	ENSP00000500828.1:p.Trp381Leu
ENST00000672593.1:c.*1368G>T	ENSP00000500455.1:n.*1368G>T
ENST00000672818.2:c.1217G>T	ENSP00000500891.1:p.Trp406Leu
ENST00000673134.1:c.*839G>T	ENSP00000500526.1:n.*839G>T
ENST00000354383.10:c.1145G>T	ENSP00000346354.6:p.Trp382Leu
ENST00000355498.6:c.1142G>T	ENSP00000347685.2:p.Trp381Leu
ENST00000372098.7:c.1217G>T	ENSP00000361170.3:p.Trp406Leu
ENST00000372104.5:c.1142G>T	ENSP00000361176.1:p.Trp381Leu
ENST00000372110.7:c.1187G>T	ENSP00000361182.3:p.Trp396Leu
ENST00000372115.7:c.1184G>T	ENSP00000361187.3:p.Trp395Leu
ENST00000448481.5:c.1175G>T	ENSP00000409718.1:p.Trp392Leu
ENST00000450313.5:c.1226G>T	ENSP00000408176.1:p.Trp409Leu
ENST00000456914.6:c.1142G>T	ENSP00000407590.2:p.Trp381Leu
ENST00000467459.5:c.559G>T	ENSP00000435889.1:n.559G>T
ENST00000475516.5:c.*955G>T	ENSP00000433843.1:n.*955G>T
ENST00000481571.5:c.*955G>T	ENSP00000436597.1:n.*955G>T
ENST00000482094.5:n.463G>T
ENST00000488731.6:c.227G>T	ENSP00000432330.1:p.Trp76Leu
ENST00000528013.6:c.1184G>T	ENSP00000433130.2:p.Trp395Leu
ENST00000529892.5:c.217G>T
ENST00000529984.5:c.227G>T	ENSP00000437093.1:p.Trp76Leu
ENST00000531105.5:c.116-2080G>T	ENSP00000431292.1:n.116-2080G>T
ENST00000533178.5:c.771G>T	ENSP00000436430.1:n.771G>T
NM_001048171.1:c.1184G>T	NP_001041636.1:p.Trp395Leu
NM_001048172.1:c.1145G>T	NP_001041637.1:p.Trp382Leu
NM_001048173.1:c.1142G>T	NP_001041638.1:p.Trp381Leu
NM_001048174.1:c.1142G>T	NP_001041639.1:p.Trp381Leu
NM_001128425.1:c.1226G>T , LRG_220t1:c.1226G>T	NP_001121897.1:p.Trp409Leu
NM_001293190.1:c.1187G>T	NP_001280119.1:p.Trp396Leu
NM_001293191.1:c.1175G>T	NP_001280120.1:p.Trp392Leu
NM_001293192.1:c.866G>T	NP_001280121.1:p.Trp289Leu
NM_001293195.1:c.1142G>T	NP_001280124.1:p.Trp381Leu
NM_001293196.1:c.866G>T	NP_001280125.1:p.Trp289Leu
NM_012222.2:c.1217G>T	NP_036354.1:p.Trp406Leu
XM_011541497.1:c.1202G>T	XP_011539799.1:p.Trp401Leu
XM_011541498.1:c.1184G>T	XP_011539800.1:p.Trp395Leu
XM_011541499.1:c.1184G>T	XP_011539801.1:p.Trp395Leu
XM_011541500.1:c.1184G>T	XP_011539802.1:p.Trp395Leu
XM_011541501.1:c.1184G>T	XP_011539803.1:p.Trp395Leu
XM_011541502.1:c.1184G>T	XP_011539804.1:p.Trp395Leu
XM_011541503.1:c.1184G>T	XP_011539805.1:p.Trp395Leu
XM_011541504.1:c.1175G>T	XP_011539806.1:p.Trp392Leu
XM_011541505.1:c.764G>T	XP_011539807.1:p.Trp255Leu
XM_011541506.1:c.764G>T	XP_011539808.1:p.Trp255Leu
XM_011541507.1:c.755G>T	XP_011539809.1:p.Trp252Leu
XM_011541508.1:c.770G>T	XP_011539810.1:p.Trp257Leu
XR_946658.1:n.1273G>T
NM_001350650.1:c.797G>T	NP_001337579.1:p.Trp266Leu
NM_001350651.1:c.797G>T	NP_001337580.1:p.Trp266Leu
NR_146882.1:n.1400G>T
NR_146883.1:n.1214G>T
XM_011541497.3:c.1202G>T	XP_011539799.1:p.Trp401Leu
XM_011541500.3:c.1184G>T	XP_011539802.1:p.Trp395Leu
XM_011541501.2:c.1184G>T	XP_011539803.1:p.Trp395Leu
XM_011541502.2:c.1184G>T	XP_011539804.1:p.Trp395Leu
XM_011541503.2:c.1184G>T	XP_011539805.1:p.Trp395Leu
XM_011541504.2:c.1175G>T	XP_011539806.1:p.Trp392Leu
XM_011541505.2:c.764G>T	XP_011539807.1:p.Trp255Leu
XM_011541506.2:c.764G>T	XP_011539808.1:p.Trp255Leu
XM_017001331.1:c.1184G>T	XP_016856820.1:p.Trp395Leu
XM_017001332.1:c.1184G>T	XP_016856821.1:p.Trp395Leu
XM_017001333.1:c.1184G>T	XP_016856822.1:p.Trp395Leu
XM_017001334.1:c.1145G>T	XP_016856823.1:p.Trp382Leu
XM_017001335.1:c.866G>T	XP_016856824.1:p.Trp289Leu
XM_017001336.1:c.797G>T	XP_016856825.1:p.Trp266Leu
XM_017001337.1:c.797G>T	XP_016856826.1:p.Trp266Leu
XM_024447244.1:c.797G>T	XP_024303012.1:p.Trp266Leu
XM_024447245.1:c.797G>T	XP_024303013.1:p.Trp266Leu
XM_024447248.1:c.755G>T	XP_024303016.1:p.Trp252Leu
XM_024447249.1:c.626G>T	XP_024303017.1:p.Trp209Leu
XM_024447250.1:c.626G>T	XP_024303018.1:p.Trp209Leu
XM_024447251.1:c.626G>T	XP_024303019.1:p.Trp209Leu
XR_001737190.1:n.1187G>T
XR_001737192.1:n.999G>T
XR_002956643.1:n.1179G>T
XR_002956644.1:n.1714G>T
XR_946658.2:n.1287G>T
NM_001048171.2:c.1142G>T	NP_001041636.2:p.Trp381Leu
NM_001128425.2:c.1226G>T MANE Plus Clinical	NP_001121897.1:p.Trp409Leu
NM_001048172.2:c.1145G>T	NP_001041637.1:p.Trp382Leu
NM_001048173.2:c.1142G>T	NP_001041638.1:p.Trp381Leu
NM_001048174.2:c.1142G>T MANE Select	NP_001041639.1:p.Trp381Leu
NM_001293190.2:c.1187G>T	NP_001280119.1:p.Trp396Leu
NM_001293191.2:c.1175G>T	NP_001280120.1:p.Trp392Leu
NM_001293192.2:c.866G>T	NP_001280121.1:p.Trp289Leu
NM_001293195.2:c.1142G>T	NP_001280124.1:p.Trp381Leu
NM_001293196.2:c.866G>T	NP_001280125.1:p.Trp289Leu
NM_001350650.2:c.797G>T	NP_001337579.1:p.Trp266Leu
NM_001350651.2:c.797G>T	NP_001337580.1:p.Trp266Leu
NM_012222.3:c.1217G>T	NP_036354.1:p.Trp406Leu
NR_146882.2:n.1370G>T
NR_146883.2:n.1219G>T