Canonical Allele Identifier: CA352134249

Gene: MYD88

Linked Data

• MyVariant Identifiers: chr3:g.38182632A>T (hg19) ; chr3:g.38141141A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38141141A>T , CM000665.2:g.38141141A>T	GRCh38
NC_000003.11:g.38182632A>T , CM000665.1:g.38182632A>T	GRCh37
NC_000003.10:g.38157636A>T	NCBI36
NG_016964.1:g.7664A>T , LRG_157:g.7664A>T
NG_023225.1:g.1102T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463956.2:n.533A>T
ENST00000484513.2:n.2224A>T
ENST00000699084.1:n.1835A>T
ENST00000699085.1:n.1611A>T
ENST00000699086.1:c.527A>T
ENST00000396334.8:c.746A>T	ENSP00000379625.4:p.Gln249Leu
ENST00000416282.3:n.849A>T
ENST00000417037.8:c.611A>T	ENSP00000401399.4:p.Gln204Leu
ENST00000421516.3:c.770A>T	ENSP00000391753.3:p.Gln257Leu
ENST00000650112.2:c.430A>T	ENSP00000497991.2:p.Arg144Ter
ENST00000650905.2:c.746A>T MANE Select	ENSP00000498360.2:p.Gln249Leu
ENST00000651800.2:c.565A>T	ENSP00000499012.2:p.Arg189Ter
ENST00000652213.1:c.727A>T	ENSP00000498576.1:p.Arg243Ter
ENST00000652590.1:n.974A>T
ENST00000396334.7:c.785A>T	ENSP00000379625.3:p.Gln262Leu
ENST00000416282.2:n.849A>T
ENST00000417037.6:c.809A>T	ENSP00000401399.2:p.Gln270Leu
ENST00000421516.1:c.806A>T	ENSP00000391753.1:p.Gln269Leu
ENST00000424893.5:c.650A>T	ENSP00000389979.1:p.Gln217Leu
ENST00000443433.6:c.604A>T	ENSP00000390565.2:p.Arg202Ter
ENST00000463956.1:n.459A>T
ENST00000481122.5:n.539A>T
ENST00000484513.1:n.1436A>T
ENST00000495303.5:c.469A>T	ENSP00000417848.1:p.Arg157Ter
NM_001172566.1:c.469A>T	NP_001166037.1:p.Arg157Ter
NM_001172567.1:c.809A>T , LRG_157t1:c.809A>T	NP_001166038.1:p.Gln270Leu
NM_001172568.1:c.650A>T	NP_001166039.1:p.Gln217Leu
NM_001172569.1:c.604A>T	NP_001166040.1:p.Arg202Ter
NM_002468.4:c.785A>T	NP_002459.2:p.Gln262Leu
XM_005265172.1:c.766A>T	XP_005265229.1:p.Arg256Ter
XM_006713170.1:c.631A>T	XP_006713233.1:p.Arg211Ter
NM_001172566.2:c.430A>T	NP_001166037.2:p.Arg144Ter
NM_001172567.2:c.770A>T	NP_001166038.2:p.Gln257Leu
NM_001172568.2:c.611A>T	NP_001166039.2:p.Gln204Leu
NM_001172569.2:c.565A>T	NP_001166040.2:p.Arg189Ter
NM_001365876.1:c.727A>T	NP_001352805.1:p.Arg243Ter
NM_001365877.1:c.592A>T	NP_001352806.1:p.Arg198Ter
NM_002468.5:c.746A>T MANE Select	NP_002459.3:p.Gln249Leu
NM_001172569.3:c.565A>T	NP_001166040.2:p.Arg189Ter
NM_001374787.1:c.703A>T	NP_001361716.1:p.Arg235Ter
NM_001374788.1:c.278A>T	NP_001361717.1:p.Gln93Leu
NR_164663.1:n.429A>T