Canonical Allele Identifier: CA352132820

Gene: MYD88

Linked Data

• MyVariant Identifiers: chr3:g.38182004G>T (hg19) ; chr3:g.38140513G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38140513G>T , CM000665.2:g.38140513G>T	GRCh38
NC_000003.11:g.38182004G>T , CM000665.1:g.38182004G>T	GRCh37
NC_000003.10:g.38157008G>T	NCBI36
NG_016964.1:g.7036G>T , LRG_157:g.7036G>T
NG_023225.1:g.1730C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.376G>T
ENST00000484513.2:n.1879G>T
ENST00000699084.1:n.1490G>T
ENST00000699085.1:n.1454G>T
ENST00000699086.1:c.389G>T
ENST00000396334.8:c.589G>T	ENSP00000379625.4:p.Asp197Tyr
ENST00000416282.3:n.504G>T
ENST00000417037.8:c.454G>T	ENSP00000401399.4:p.Asp152Tyr
ENST00000421516.3:c.589G>T	ENSP00000391753.3:p.Asp197Tyr
ENST00000650112.2:c.329-244G>T	ENSP00000497991.2:n.329-244G>T
ENST00000650905.2:c.589G>T MANE Select	ENSP00000498360.2:p.Asp197Tyr
ENST00000651800.2:c.464-244G>T	ENSP00000499012.2:n.464-244G>T
ENST00000652213.1:c.589G>T	ENSP00000498576.1:p.Asp197Tyr
ENST00000652590.1:n.629G>T
ENST00000396334.7:c.628G>T	ENSP00000379625.3:p.Asp210Tyr
ENST00000416282.2:n.504G>T
ENST00000417037.6:c.628G>T	ENSP00000401399.2:p.Asp210Tyr
ENST00000421516.1:c.625G>T	ENSP00000391753.1:p.Asp209Tyr
ENST00000424893.5:c.493G>T	ENSP00000389979.1:p.Asp165Tyr
ENST00000443433.6:c.503-244G>T	ENSP00000390565.2:n.503-244G>T
ENST00000460295.1:n.1022G>T
ENST00000463956.1:n.302G>T
ENST00000481122.5:n.382G>T
ENST00000484513.1:n.1091G>T
ENST00000495303.5:c.368-244G>T	ENSP00000417848.1:n.368-244G>T
NM_001172566.1:c.368-244G>T	NP_001166037.1:n.368-244G>T
NM_001172567.1:c.628G>T , LRG_157t1:c.628G>T	NP_001166038.1:p.Asp210Tyr
NM_001172568.1:c.493G>T	NP_001166039.1:p.Asp165Tyr
NM_001172569.1:c.503-244G>T	NP_001166040.1:n.503-244G>T
NM_002468.4:c.628G>T	NP_002459.2:p.Asp210Tyr
XM_005265172.1:c.628G>T	XP_005265229.1:p.Asp210Tyr
XM_006713170.1:c.493G>T	XP_006713233.1:p.Asp165Tyr
NM_001172566.2:c.329-244G>T	NP_001166037.2:n.329-244G>T
NM_001172567.2:c.589G>T	NP_001166038.2:p.Asp197Tyr
NM_001172568.2:c.454G>T	NP_001166039.2:p.Asp152Tyr
NM_001172569.2:c.464-244G>T	NP_001166040.2:n.464-244G>T
NM_001365876.1:c.589G>T	NP_001352805.1:p.Asp197Tyr
NM_001365877.1:c.454G>T	NP_001352806.1:p.Asp152Tyr
NM_002468.5:c.589G>T MANE Select	NP_002459.3:p.Asp197Tyr
NM_001172569.3:c.464-244G>T	NP_001166040.2:n.464-244G>T
NM_001374787.1:c.589G>T	NP_001361716.1:p.Asp197Tyr
NM_001374788.1:c.121G>T	NP_001361717.1:p.Asp41Tyr
NR_164663.1:n.291G>T