Canonical Allele Identifier: CA012548

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 185327
• ClinVar RCV Id: RCV000164727 ; RCV000204019 ; RCV001589030
• dbSNP Id: rs751465584
• ExAC: 1:45797113 C / T
• gnomAD v2: 1-45797113-C-T
• gnomAD v3: 1-45331441-C-T
• gnomAD v4: 1-45331441-C-T
• MyVariant Identifiers: chr1:g.45797113C>T (hg19) ; chr1:g.45331441C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45331441C>T , CM000663.2:g.45331441C>T	GRCh38
NC_000001.10:g.45797113C>T , CM000663.1:g.45797113C>T	GRCh37
NC_000001.9:g.45569700C>T	NCBI36
NG_008189.1:g.14030G>A , LRG_220:g.14030G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.834G>A	ENSP00000410263.2:p.Thr278=
ENST00000435155.2:c.1251G>A	ENSP00000403655.2:p.Thr417=
ENST00000467459.6:c.*80G>A	ENSP00000435889.2:n.*80G>A
ENST00000483127.2:c.1236G>A	ENSP00000436469.2:p.Thr412=
ENST00000485271.6:c.1218G>A	ENSP00000431264.2:p.Thr406=
ENST00000529892.6:c.1071G>A	ENSP00000432528.2:p.Thr357=
ENST00000533178.6:c.*547G>A	ENSP00000436430.2:n.*547G>A
ENST00000672314.2:c.1218G>A	ENSP00000500828.2:p.Thr406=
ENST00000710952.2:c.1302G>A MANE Plus Clinical	ENSP00000518552.2:p.Thr434=
ENST00000672818.3:c.1293G>A	ENSP00000500891.1:p.Thr431=
ENST00000456914.7:c.1218G>A MANE Select	ENSP00000407590.2:p.Thr406=
ENST00000671898.1:c.1806G>A	ENSP00000499896.1:p.Thr602=
ENST00000672011.1:c.*547G>A	ENSP00000500418.1:n.*547G>A
ENST00000672314.1:c.1218G>A	ENSP00000500828.1:p.Thr406=
ENST00000672593.1:c.*1444G>A	ENSP00000500455.1:n.*1444G>A
ENST00000672818.2:c.1293G>A	ENSP00000500891.1:p.Thr431=
ENST00000673134.1:c.*915G>A	ENSP00000500526.1:n.*915G>A
ENST00000354383.10:c.1221G>A	ENSP00000346354.6:p.Thr407=
ENST00000355498.6:c.1218G>A	ENSP00000347685.2:p.Thr406=
ENST00000372098.7:c.1293G>A	ENSP00000361170.3:p.Thr431=
ENST00000372104.5:c.1218G>A	ENSP00000361176.1:p.Thr406=
ENST00000372110.7:c.1263G>A	ENSP00000361182.3:p.Thr421=
ENST00000372115.7:c.1260G>A	ENSP00000361187.3:p.Thr420=
ENST00000448481.5:c.1251G>A	ENSP00000409718.1:p.Thr417=
ENST00000450313.5:c.1302G>A	ENSP00000408176.1:p.Thr434=
ENST00000456914.6:c.1218G>A	ENSP00000407590.2:p.Thr406=
ENST00000467459.5:c.635G>A	ENSP00000435889.1:n.635G>A
ENST00000475516.5:c.*1031G>A	ENSP00000433843.1:n.*1031G>A
ENST00000481571.5:c.*1031G>A	ENSP00000436597.1:n.*1031G>A
ENST00000482094.5:n.539G>A
ENST00000488731.6:c.303G>A	ENSP00000432330.1:p.Thr101=
ENST00000528013.6:c.1260G>A	ENSP00000433130.2:p.Thr420=
ENST00000529892.5:c.293G>A
ENST00000529984.5:c.303G>A	ENSP00000437093.1:p.Thr101=
ENST00000531105.5:c.116-2004G>A	ENSP00000431292.1:n.116-2004G>A
ENST00000533178.5:c.847G>A	ENSP00000436430.1:n.847G>A
NM_001048171.1:c.1260G>A	NP_001041636.1:p.Thr420=
NM_001048172.1:c.1221G>A	NP_001041637.1:p.Thr407=
NM_001048173.1:c.1218G>A	NP_001041638.1:p.Thr406=
NM_001048174.1:c.1218G>A	NP_001041639.1:p.Thr406=
NM_001128425.1:c.1302G>A , LRG_220t1:c.1302G>A	NP_001121897.1:p.Thr434=
NM_001293190.1:c.1263G>A	NP_001280119.1:p.Thr421=
NM_001293191.1:c.1251G>A	NP_001280120.1:p.Thr417=
NM_001293192.1:c.942G>A	NP_001280121.1:p.Thr314=
NM_001293195.1:c.1218G>A	NP_001280124.1:p.Thr406=
NM_001293196.1:c.942G>A	NP_001280125.1:p.Thr314=
NM_012222.2:c.1293G>A	NP_036354.1:p.Thr431=
XM_011541497.1:c.1278G>A	XP_011539799.1:p.Thr426=
XM_011541498.1:c.1260G>A	XP_011539800.1:p.Thr420=
XM_011541499.1:c.1260G>A	XP_011539801.1:p.Thr420=
XM_011541500.1:c.1260G>A	XP_011539802.1:p.Thr420=
XM_011541501.1:c.1260G>A	XP_011539803.1:p.Thr420=
XM_011541502.1:c.1260G>A	XP_011539804.1:p.Thr420=
XM_011541503.1:c.1260G>A	XP_011539805.1:p.Thr420=
XM_011541504.1:c.1251G>A	XP_011539806.1:p.Thr417=
XM_011541505.1:c.840G>A	XP_011539807.1:p.Thr280=
XM_011541506.1:c.840G>A	XP_011539808.1:p.Thr280=
XM_011541507.1:c.831G>A	XP_011539809.1:p.Thr277=
XM_011541508.1:c.846G>A	XP_011539810.1:p.Thr282=
XR_946658.1:n.1349G>A
NM_001350650.1:c.873G>A	NP_001337579.1:p.Thr291=
NM_001350651.1:c.873G>A	NP_001337580.1:p.Thr291=
NR_146882.1:n.1476G>A
NR_146883.1:n.1290G>A
XM_011541497.3:c.1278G>A	XP_011539799.1:p.Thr426=
XM_011541500.3:c.1260G>A	XP_011539802.1:p.Thr420=
XM_011541501.2:c.1260G>A	XP_011539803.1:p.Thr420=
XM_011541502.2:c.1260G>A	XP_011539804.1:p.Thr420=
XM_011541503.2:c.1260G>A	XP_011539805.1:p.Thr420=
XM_011541504.2:c.1251G>A	XP_011539806.1:p.Thr417=
XM_011541505.2:c.840G>A	XP_011539807.1:p.Thr280=
XM_011541506.2:c.840G>A	XP_011539808.1:p.Thr280=
XM_017001331.1:c.1260G>A	XP_016856820.1:p.Thr420=
XM_017001332.1:c.1260G>A	XP_016856821.1:p.Thr420=
XM_017001333.1:c.1260G>A	XP_016856822.1:p.Thr420=
XM_017001334.1:c.1221G>A	XP_016856823.1:p.Thr407=
XM_017001335.1:c.942G>A	XP_016856824.1:p.Thr314=
XM_017001336.1:c.873G>A	XP_016856825.1:p.Thr291=
XM_017001337.1:c.873G>A	XP_016856826.1:p.Thr291=
XM_024447244.1:c.873G>A	XP_024303012.1:p.Thr291=
XM_024447245.1:c.873G>A	XP_024303013.1:p.Thr291=
XM_024447248.1:c.831G>A	XP_024303016.1:p.Thr277=
XM_024447249.1:c.702G>A	XP_024303017.1:p.Thr234=
XM_024447250.1:c.702G>A	XP_024303018.1:p.Thr234=
XM_024447251.1:c.702G>A	XP_024303019.1:p.Thr234=
XR_001737190.1:n.1263G>A
XR_001737192.1:n.1075G>A
XR_002956643.1:n.1255G>A
XR_002956644.1:n.1790G>A
XR_946658.2:n.1363G>A
NM_001048171.2:c.1218G>A	NP_001041636.2:p.Thr406=
NM_001128425.2:c.1302G>A MANE Plus Clinical	NP_001121897.1:p.Thr434=
NM_001048172.2:c.1221G>A	NP_001041637.1:p.Thr407=
NM_001048173.2:c.1218G>A	NP_001041638.1:p.Thr406=
NM_001048174.2:c.1218G>A MANE Select	NP_001041639.1:p.Thr406=
NM_001293190.2:c.1263G>A	NP_001280119.1:p.Thr421=
NM_001293191.2:c.1251G>A	NP_001280120.1:p.Thr417=
NM_001293192.2:c.942G>A	NP_001280121.1:p.Thr314=
NM_001293195.2:c.1218G>A	NP_001280124.1:p.Thr406=
NM_001293196.2:c.942G>A	NP_001280125.1:p.Thr314=
NM_001350650.2:c.873G>A	NP_001337579.1:p.Thr291=
NM_001350651.2:c.873G>A	NP_001337580.1:p.Thr291=
NM_012222.3:c.1293G>A	NP_036354.1:p.Thr431=
NR_146882.2:n.1446G>A
NR_146883.2:n.1295G>A