Canonical Allele Identifier: CA645530353

Gene: MYD88

Linked Data

• COSMIC: COSM5010441

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38141148_38141150delinsGCGGCCCCC , CM000665.2:g.38141148_38141150delinsGCGGCCCCC	GRCh38
NC_000003.11:g.38182639_38182641delinsGCGGCCCCC , CM000665.1:g.38182639_38182641delinsGCGGCCCCC	GRCh37
NC_000003.10:g.38157643_38157645delinsGCGGCCCCC	NCBI36
NG_016964.1:g.7671_7673delinsGCGGCCCCC , LRG_157:g.7671_7673delinsGCGGCCCCC
NG_023225.1:g.1093_1095delinsGGGGGCCGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.540_542delinsGCGGCCCCC
ENST00000484513.2:n.2231_2233delinsGCGGCCCCC
ENST00000699084.1:n.1842_1844delinsGCGGCCCCC
ENST00000699085.1:n.1618_1620delinsGCGGCCCCC
ENST00000699086.1:c.534_536delinsGCGGCCCCC
ENST00000396334.8:c.753_755delinsGCGGCCCCC	ENSP00000379625.4:p.Leu252delinsArgProPro
ENST00000416282.3:n.856_858delinsGCGGCCCCC
ENST00000417037.8:c.618_620delinsGCGGCCCCC	ENSP00000401399.4:p.Leu207delinsArgProPro
ENST00000421516.3:c.777_779delinsGCGGCCCCC	ENSP00000391753.3:p.Leu260delinsArgProPro
ENST00000650112.2:c.437_439delinsGCGGCCCCC	ENSP00000497991.2:p.Asp146_Ter147delinsGlyGlyProArg
ENST00000650905.2:c.753_755delinsGCGGCCCCC MANE Select	ENSP00000498360.2:p.Leu252delinsArgProPro
ENST00000651800.2:c.572_574delinsGCGGCCCCC	ENSP00000499012.2:p.Asp191_Ter192delinsGlyGlyProArg
ENST00000652213.1:c.734_736delinsGCGGCCCCC	ENSP00000498576.1:p.Asp245_Ter246delinsGlyGlyProArg
ENST00000652590.1:n.981_983delinsGCGGCCCCC
ENST00000396334.7:c.792_794delinsGCGGCCCCC	ENSP00000379625.3:p.Leu265delinsArgProPro
ENST00000416282.2:n.856_858delinsGCGGCCCCC
ENST00000417037.6:c.816_818delinsGCGGCCCCC	ENSP00000401399.2:p.Leu273delinsArgProPro
ENST00000421516.1:c.813_815delinsGCGGCCCCC	ENSP00000391753.1:p.Leu272delinsArgProPro
ENST00000424893.5:c.657_659delinsGCGGCCCCC	ENSP00000389979.1:p.Leu220delinsArgProPro
ENST00000443433.6:c.611_613delinsGCGGCCCCC	ENSP00000390565.2:p.Asp204_Ter205delinsGlyGlyProArg
ENST00000463956.1:n.466_468delinsGCGGCCCCC
ENST00000481122.5:n.546_548delinsGCGGCCCCC
ENST00000484513.1:n.1443_1445delinsGCGGCCCCC
ENST00000495303.5:c.476_478delinsGCGGCCCCC	ENSP00000417848.1:p.Asp159_Ter160delinsGlyGlyProArg
NM_001172566.1:c.476_478delinsGCGGCCCCC	NP_001166037.1:p.Asp159_Ter160delinsGlyGlyProArg
NM_001172567.1:c.816_818delinsGCGGCCCCC , LRG_157t1:c.816_818delinsGCGGCCCCC	NP_001166038.1:p.Leu273delinsArgProPro
NM_001172568.1:c.657_659delinsGCGGCCCCC	NP_001166039.1:p.Leu220delinsArgProPro
NM_001172569.1:c.611_613delinsGCGGCCCCC	NP_001166040.1:p.Asp204_Ter205delinsGlyGlyProArg
NM_002468.4:c.792_794delinsGCGGCCCCC	NP_002459.2:p.Leu265delinsArgProPro
XM_005265172.1:c.773_775delinsGCGGCCCCC	XP_005265229.1:p.Asp258_Ter259delinsGlyGlyProArg
XM_006713170.1:c.638_640delinsGCGGCCCCC	XP_006713233.1:p.Asp213_Ter214delinsGlyGlyProArg
NM_001172566.2:c.437_439delinsGCGGCCCCC	NP_001166037.2:p.Asp146_Ter147delinsGlyGlyProArg
NM_001172567.2:c.777_779delinsGCGGCCCCC	NP_001166038.2:p.Leu260delinsArgProPro
NM_001172568.2:c.618_620delinsGCGGCCCCC	NP_001166039.2:p.Leu207delinsArgProPro
NM_001172569.2:c.572_574delinsGCGGCCCCC	NP_001166040.2:p.Asp191_Ter192delinsGlyGlyProArg
NM_001365876.1:c.734_736delinsGCGGCCCCC	NP_001352805.1:p.Asp245_Ter246delinsGlyGlyProArg
NM_001365877.1:c.599_601delinsGCGGCCCCC	NP_001352806.1:p.Asp200_Ter201delinsGlyGlyProArg
NM_002468.5:c.753_755delinsGCGGCCCCC MANE Select	NP_002459.3:p.Leu252delinsArgProPro
NM_001172569.3:c.572_574delinsGCGGCCCCC	NP_001166040.2:p.Asp191_Ter192delinsGlyGlyProArg
NM_001374787.1:c.710_712delinsGCGGCCCCC	NP_001361716.1:p.Asp237_Ter238delinsGlyGlyProArg
NM_001374788.1:c.285_287delinsGCGGCCCCC	NP_001361717.1:p.Leu96delinsArgProPro
NR_164663.1:n.436_438delinsGCGGCCCCC