Canonical Allele Identifier: CA340137857

Gene: MUTYH TOE1

Linked Data

• MyVariant Identifiers: chr1:g.45805901C>G (hg19) ; chr1:g.45340229C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45340229C>G , CM000663.2:g.45340229C>G	GRCh38
NC_000001.10:g.45805901C>G , CM000663.1:g.45805901C>G	GRCh37
NC_000001.9:g.45578488C>G	NCBI36
NG_008189.1:g.5242G>C , LRG_220:g.5242G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.26G>C (MUTYH)	ENSP00000410263.2:p.Ser9Thr
ENST00000529892.6:c.26G>C (MUTYH)	ENSP00000432528.2:p.Ser9Thr
ENST00000710952.2:c.26G>C (MUTYH) MANE Plus Clinical	ENSP00000518552.2:p.Ser9Thr
ENST00000672818.3:c.26G>C (MUTYH)	ENSP00000500891.1:p.Ser9Thr
ENST00000372090.6:c.-24C>G (TOE1) MANE Select	ENSP00000361162.5:n.-24C>G
ENST00000450313.6:c.26G>C (MUTYH)	ENSP00000408176.2:p.Ser9Thr
ENST00000461495.6:c.26G>C (MUTYH)	ENSP00000437166.1:p.Ser9Thr
ENST00000671856.1:n.4G>C (MUTYH)
ENST00000671898.1:c.541-5718G>C	ENSP00000499896.1:n.541-5718G>C
ENST00000672011.1:c.26G>C (MUTYH)	ENSP00000500418.1:p.Ser9Thr
ENST00000672818.2:c.26G>C (MUTYH)	ENSP00000500891.1:p.Ser9Thr
ENST00000372090.5:c.-24C>G (TOE1)	ENSP00000361162.5:n.-24C>G
ENST00000372098.7:c.26G>C (MUTYH)	ENSP00000361170.3:p.Ser9Thr
ENST00000372110.7:c.26G>C (MUTYH)	ENSP00000361182.3:p.Ser9Thr
ENST00000372115.7:c.26G>C (MUTYH)	ENSP00000361187.3:p.Ser9Thr
ENST00000412971.5:c.26G>C (MUTYH)	ENSP00000410263.1:p.Ser9Thr
ENST00000450313.5:c.26G>C (MUTYH)	ENSP00000408176.1:p.Ser9Thr
ENST00000461495.5:c.26G>C (MUTYH)	ENSP00000437166.1:p.Ser9Thr
ENST00000462387.5:n.204G>C (MUTYH)
ENST00000467940.5:c.26G>C (MUTYH)	ENSP00000436478.1:p.Ser9Thr
ENST00000471337.5:n.55C>G (TOE1)
ENST00000476789.5:n.204G>C (MUTYH)
ENST00000477731.5:n.178C>G (TOE1)
ENST00000481139.5:n.187G>C (MUTYH)
ENST00000481571.5:c.26G>C (MUTYH)	ENSP00000436597.1:p.Ser9Thr
ENST00000483642.5:n.169G>C (MUTYH)
ENST00000495703.5:n.9C>G (TOE1)
ENST00000525160.5:c.26G>C (MUTYH)	ENSP00000431568.1:p.Ser9Thr
ENST00000529984.5:c.-17G>C (MUTYH)	ENSP00000437093.1:n.-17G>C
ENST00000534453.1:n.7G>C (MUTYH)
NM_001048171.1:c.26G>C (MUTYH)	NP_001041636.1:p.Ser9Thr
NM_001128425.1:c.26G>C , LRG_220t1:c.26G>C (MUTYH)	NP_001121897.1:p.Ser9Thr
NM_001293190.1:c.26G>C (MUTYH)	NP_001280119.1:p.Ser9Thr
NM_001293192.1:c.-229G>C (MUTYH)	NP_001280121.1:n.-229G>C
NM_012222.2:c.26G>C (MUTYH)	NP_036354.1:p.Ser9Thr
NM_025077.3:c.-24C>G (TOE1)	NP_079353.3:n.-24C>G
XM_005270412.2:c.-24C>G (TOE1)	XP_005270469.1:n.-24C>G
XM_005270413.3:c.-400C>G (TOE1)	XP_005270470.1:n.-400C>G
XM_011540569.1:c.-308C>G (TOE1)	XP_011538871.1:n.-308C>G
XM_011541503.1:c.26G>C (MUTYH)	XP_011539805.1:p.Ser9Thr
XM_011541505.1:c.-90G>C (MUTYH)	XP_011539807.1:n.-90G>C
XR_246230.2:n.254C>G (TOE1)
XR_426587.2:n.56C>G (TOE1)
XR_946532.1:n.56C>G (TOE1)
XR_946658.1:n.73G>C (MUTYH)
NM_001350650.1:c.-288G>C (MUTYH)	NP_001337579.1:n.-288G>C
NM_001350651.1:c.-224G>C (MUTYH)	NP_001337580.1:n.-224G>C
NR_146882.1:n.242G>C (MUTYH)
XM_005270412.4:c.-24C>G (TOE1)	XP_005270469.1:n.-24C>G
XM_005270413.5:c.-400C>G (TOE1)	XP_005270470.1:n.-400C>G
XM_011540569.3:c.-308C>G (TOE1)	XP_011538871.1:n.-308C>G
XM_011541503.2:c.26G>C (MUTYH)	XP_011539805.1:p.Ser9Thr
XM_011541505.2:c.-90G>C (MUTYH)	XP_011539807.1:n.-90G>C
XM_017001331.1:c.-33G>C (MUTYH)	XP_016856820.1:n.-33G>C
XM_017001332.1:c.-13G>C (MUTYH)	XP_016856821.1:n.-13G>C
XM_017001335.1:c.-245G>C (MUTYH)	XP_016856824.1:n.-245G>C
XM_017001336.1:c.-321G>C (MUTYH)	XP_016856825.1:n.-321G>C
XM_024447244.1:c.-330G>C (MUTYH)	XP_024303012.1:n.-330G>C
XM_024447248.1:c.-288G>C (MUTYH)	XP_024303016.1:n.-288G>C
XM_024447249.1:c.-780G>C (MUTYH)	XP_024303017.1:n.-780G>C
XM_024447250.1:c.-803G>C (MUTYH)	XP_024303018.1:n.-803G>C
XM_024452837.1:c.-400C>G (TOE1)	XP_024308605.1:n.-400C>G
XR_001736951.2:n.164C>G (TOE1)
XR_001737190.1:n.93G>C (MUTYH)
XR_002956643.1:n.201G>C (MUTYH)
XR_002956644.1:n.219G>C (MUTYH)
XR_002959287.1:n.479C>G (TOE1)
XR_246230.4:n.164C>G (TOE1)
XR_426587.4:n.56C>G (TOE1)
XR_946532.3:n.56C>G (TOE1)
XR_946658.2:n.87G>C (MUTYH)
NM_025077.4:c.-24C>G (TOE1) MANE Select	NP_079353.3:n.-24C>G
NM_001048171.2:c.-17G>C (MUTYH)	NP_001041636.2:n.-17G>C
NM_001128425.2:c.26G>C (MUTYH) MANE Plus Clinical	NP_001121897.1:p.Ser9Thr
NM_001293190.2:c.26G>C (MUTYH)	NP_001280119.1:p.Ser9Thr
NM_001293192.2:c.-229G>C (MUTYH)	NP_001280121.1:n.-229G>C
NM_001350650.2:c.-288G>C (MUTYH)	NP_001337579.1:n.-288G>C
NM_001350651.2:c.-224G>C (MUTYH)	NP_001337580.1:n.-224G>C
NM_012222.3:c.26G>C (MUTYH)	NP_036354.1:p.Ser9Thr
NR_146882.2:n.212G>C (MUTYH)