Canonical Allele Identifier: CA340131863

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 492022
• ClinVar RCV Id: RCV000584133
• dbSNP Id: rs1553123034
• gnomAD v3: 1-45329410-G-T
• gnomAD v4: 1-45329410-G-T
• MyVariant Identifiers: chr1:g.45795082G>T (hg19) ; chr1:g.45329410G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45329410G>T , CM000663.2:g.45329410G>T	GRCh38
NC_000001.10:g.45795082G>T , CM000663.1:g.45795082G>T	GRCh37
NC_000001.9:g.45567669G>T	NCBI36
NG_008189.1:g.16061C>A , LRG_220:g.16061C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.1078C>A	ENSP00000410263.2:p.Pro360Thr
ENST00000435155.2:c.1495C>A	ENSP00000403655.2:p.Pro499Thr
ENST00000467459.6:c.*324C>A	ENSP00000435889.2:n.*324C>A
ENST00000483127.2:c.1480C>A	ENSP00000436469.2:p.Pro494Thr
ENST00000485271.6:c.*205C>A	ENSP00000431264.2:n.*205C>A
ENST00000529892.6:c.1315C>A	ENSP00000432528.2:p.Pro439Thr
ENST00000533178.6:c.*791C>A	ENSP00000436430.2:n.*791C>A
ENST00000672314.2:c.1462C>A	ENSP00000500828.2:p.Pro488Thr
ENST00000710952.2:c.1546C>A MANE Plus Clinical	ENSP00000518552.2:p.Pro516Thr
ENST00000672818.3:c.1537C>A	ENSP00000500891.1:p.Pro513Thr
ENST00000456914.7:c.1462C>A MANE Select	ENSP00000407590.2:p.Pro488Thr
ENST00000671898.1:c.*205C>A	ENSP00000499896.1:n.*205C>A
ENST00000672011.1:c.*791C>A	ENSP00000500418.1:n.*791C>A
ENST00000672818.2:c.1537C>A	ENSP00000500891.1:p.Pro513Thr
ENST00000354383.10:c.1465C>A	ENSP00000346354.6:p.Pro489Thr
ENST00000355498.6:c.1462C>A	ENSP00000347685.2:p.Pro488Thr
ENST00000372098.7:c.1537C>A	ENSP00000361170.3:p.Pro513Thr
ENST00000372104.5:c.1462C>A	ENSP00000361176.1:p.Pro488Thr
ENST00000372110.7:c.1507C>A	ENSP00000361182.3:p.Pro503Thr
ENST00000372115.7:c.1504C>A	ENSP00000361187.3:p.Pro502Thr
ENST00000448481.5:c.1495C>A	ENSP00000409718.1:p.Pro499Thr
ENST00000450313.5:c.1546C>A	ENSP00000408176.1:p.Pro516Thr
ENST00000456914.6:c.1462C>A	ENSP00000407590.2:p.Pro488Thr
ENST00000467459.5:c.879C>A	ENSP00000435889.1:n.879C>A
ENST00000475516.5:c.*1275C>A	ENSP00000433843.1:n.*1275C>A
ENST00000481571.5:c.*1275C>A	ENSP00000436597.1:n.*1275C>A
ENST00000482094.5:n.783C>A
ENST00000485271.5:c.339C>A
ENST00000488731.6:c.547C>A	ENSP00000432330.1:p.Pro183Thr
ENST00000528013.6:c.1504C>A	ENSP00000433130.2:p.Pro502Thr
ENST00000529892.5:c.537C>A
ENST00000529984.5:c.547C>A	ENSP00000437093.1:p.Pro183Thr
ENST00000531105.5:c.143C>A	ENSP00000431292.1:p.Ser48Tyr
ENST00000533178.5:c.1091C>A	ENSP00000436430.1:n.1091C>A
NM_001048171.1:c.1504C>A	NP_001041636.1:p.Pro502Thr
NM_001048172.1:c.1465C>A	NP_001041637.1:p.Pro489Thr
NM_001048173.1:c.1462C>A	NP_001041638.1:p.Pro488Thr
NM_001048174.1:c.1462C>A	NP_001041639.1:p.Pro488Thr
NM_001128425.1:c.1546C>A , LRG_220t1:c.1546C>A	NP_001121897.1:p.Pro516Thr
NM_001293190.1:c.1507C>A	NP_001280119.1:p.Pro503Thr
NM_001293191.1:c.1495C>A	NP_001280120.1:p.Pro499Thr
NM_001293192.1:c.1186C>A	NP_001280121.1:p.Pro396Thr
NM_001293195.1:c.1462C>A	NP_001280124.1:p.Pro488Thr
NM_001293196.1:c.1186C>A	NP_001280125.1:p.Pro396Thr
NM_012222.2:c.1537C>A	NP_036354.1:p.Pro513Thr
XM_011541497.1:c.1522C>A	XP_011539799.1:p.Pro508Thr
XM_011541498.1:c.1504C>A	XP_011539800.1:p.Pro502Thr
XM_011541499.1:c.1504C>A	XP_011539801.1:p.Pro502Thr
XM_011541500.1:c.1504C>A	XP_011539802.1:p.Pro502Thr
XM_011541501.1:c.1504C>A	XP_011539803.1:p.Pro502Thr
XM_011541502.1:c.1504C>A	XP_011539804.1:p.Pro502Thr
XM_011541503.1:c.1504C>A	XP_011539805.1:p.Pro502Thr
XM_011541504.1:c.1495C>A	XP_011539806.1:p.Pro499Thr
XM_011541505.1:c.1084C>A	XP_011539807.1:p.Pro362Thr
XM_011541506.1:c.1084C>A	XP_011539808.1:p.Pro362Thr
XM_011541507.1:c.1075C>A	XP_011539809.1:p.Pro359Thr
XM_011541508.1:c.1090C>A	XP_011539810.1:p.Pro364Thr
XR_946658.1:n.1773C>A
NM_001350650.1:c.1117C>A	NP_001337579.1:p.Pro373Thr
NM_001350651.1:c.1117C>A	NP_001337580.1:p.Pro373Thr
NR_146882.1:n.1900C>A
NR_146883.1:n.1714C>A
XM_011541497.3:c.1522C>A	XP_011539799.1:p.Pro508Thr
XM_011541500.3:c.1504C>A	XP_011539802.1:p.Pro502Thr
XM_011541501.2:c.1504C>A	XP_011539803.1:p.Pro502Thr
XM_011541502.2:c.1504C>A	XP_011539804.1:p.Pro502Thr
XM_011541503.2:c.1504C>A	XP_011539805.1:p.Pro502Thr
XM_011541504.2:c.1495C>A	XP_011539806.1:p.Pro499Thr
XM_011541505.2:c.1084C>A	XP_011539807.1:p.Pro362Thr
XM_011541506.2:c.1084C>A	XP_011539808.1:p.Pro362Thr
XM_017001331.1:c.1504C>A	XP_016856820.1:p.Pro502Thr
XM_017001332.1:c.1504C>A	XP_016856821.1:p.Pro502Thr
XM_017001333.1:c.1504C>A	XP_016856822.1:p.Pro502Thr
XM_017001334.1:c.1465C>A	XP_016856823.1:p.Pro489Thr
XM_017001335.1:c.1186C>A	XP_016856824.1:p.Pro396Thr
XM_017001336.1:c.1117C>A	XP_016856825.1:p.Pro373Thr
XM_017001337.1:c.1117C>A	XP_016856826.1:p.Pro373Thr
XM_024447244.1:c.1117C>A	XP_024303012.1:p.Pro373Thr
XM_024447245.1:c.1117C>A	XP_024303013.1:p.Pro373Thr
XM_024447248.1:c.1075C>A	XP_024303016.1:p.Pro359Thr
XM_024447249.1:c.946C>A	XP_024303017.1:p.Pro316Thr
XM_024447250.1:c.946C>A	XP_024303018.1:p.Pro316Thr
XM_024447251.1:c.946C>A	XP_024303019.1:p.Pro316Thr
XR_001737190.1:n.1687C>A
XR_001737192.1:n.1499C>A
XR_002956643.1:n.1679C>A
XR_002956644.1:n.2214C>A
XR_946658.2:n.1787C>A
NM_001048171.2:c.1462C>A	NP_001041636.2:p.Pro488Thr
NM_001128425.2:c.1546C>A MANE Plus Clinical	NP_001121897.1:p.Pro516Thr
NM_001048172.2:c.1465C>A	NP_001041637.1:p.Pro489Thr
NM_001048173.2:c.1462C>A	NP_001041638.1:p.Pro488Thr
NM_001048174.2:c.1462C>A MANE Select	NP_001041639.1:p.Pro488Thr
NM_001293190.2:c.1507C>A	NP_001280119.1:p.Pro503Thr
NM_001293191.2:c.1495C>A	NP_001280120.1:p.Pro499Thr
NM_001293192.2:c.1186C>A	NP_001280121.1:p.Pro396Thr
NM_001293195.2:c.1462C>A	NP_001280124.1:p.Pro488Thr
NM_001293196.2:c.1186C>A	NP_001280125.1:p.Pro396Thr
NM_001350650.2:c.1117C>A	NP_001337579.1:p.Pro373Thr
NM_001350651.2:c.1117C>A	NP_001337580.1:p.Pro373Thr
NM_012222.3:c.1537C>A	NP_036354.1:p.Pro513Thr
NR_146882.2:n.1870C>A
NR_146883.2:n.1719C>A