Canonical Allele Identifier: CA352132832

Gene: MYD88

Linked Data

• dbSNP Id: rs2125778725
• MyVariant Identifiers: chr3:g.38182005A>T (hg19) ; chr3:g.38140514A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38140514A>T , CM000665.2:g.38140514A>T	GRCh38
NC_000003.11:g.38182005A>T , CM000665.1:g.38182005A>T	GRCh37
NC_000003.10:g.38157009A>T	NCBI36
NG_016964.1:g.7037A>T , LRG_157:g.7037A>T
NG_023225.1:g.1729T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.377A>T
ENST00000484513.2:n.1880A>T
ENST00000699084.1:n.1491A>T
ENST00000699085.1:n.1455A>T
ENST00000699086.1:c.390A>T
ENST00000396334.8:c.590A>T	ENSP00000379625.4:p.Asp197Val
ENST00000416282.3:n.505A>T
ENST00000417037.8:c.455A>T	ENSP00000401399.4:p.Asp152Val
ENST00000421516.3:c.590A>T	ENSP00000391753.3:p.Asp197Val
ENST00000650112.2:c.329-243A>T	ENSP00000497991.2:n.329-243A>T
ENST00000650905.2:c.590A>T MANE Select	ENSP00000498360.2:p.Asp197Val
ENST00000651800.2:c.464-243A>T	ENSP00000499012.2:n.464-243A>T
ENST00000652213.1:c.590A>T	ENSP00000498576.1:p.Asp197Val
ENST00000652590.1:n.630A>T
ENST00000396334.7:c.629A>T	ENSP00000379625.3:p.Asp210Val
ENST00000416282.2:n.505A>T
ENST00000417037.6:c.629A>T	ENSP00000401399.2:p.Asp210Val
ENST00000421516.1:c.626A>T	ENSP00000391753.1:p.Asp209Val
ENST00000424893.5:c.494A>T	ENSP00000389979.1:p.Asp165Val
ENST00000443433.6:c.503-243A>T	ENSP00000390565.2:n.503-243A>T
ENST00000460295.1:n.1023A>T
ENST00000463956.1:n.303A>T
ENST00000481122.5:n.383A>T
ENST00000484513.1:n.1092A>T
ENST00000495303.5:c.368-243A>T	ENSP00000417848.1:n.368-243A>T
NM_001172566.1:c.368-243A>T	NP_001166037.1:n.368-243A>T
NM_001172567.1:c.629A>T , LRG_157t1:c.629A>T	NP_001166038.1:p.Asp210Val
NM_001172568.1:c.494A>T	NP_001166039.1:p.Asp165Val
NM_001172569.1:c.503-243A>T	NP_001166040.1:n.503-243A>T
NM_002468.4:c.629A>T	NP_002459.2:p.Asp210Val
XM_005265172.1:c.629A>T	XP_005265229.1:p.Asp210Val
XM_006713170.1:c.494A>T	XP_006713233.1:p.Asp165Val
NM_001172566.2:c.329-243A>T	NP_001166037.2:n.329-243A>T
NM_001172567.2:c.590A>T	NP_001166038.2:p.Asp197Val
NM_001172568.2:c.455A>T	NP_001166039.2:p.Asp152Val
NM_001172569.2:c.464-243A>T	NP_001166040.2:n.464-243A>T
NM_001365876.1:c.590A>T	NP_001352805.1:p.Asp197Val
NM_001365877.1:c.455A>T	NP_001352806.1:p.Asp152Val
NM_002468.5:c.590A>T MANE Select	NP_002459.3:p.Asp197Val
NM_001172569.3:c.464-243A>T	NP_001166040.2:n.464-243A>T
NM_001374787.1:c.590A>T	NP_001361716.1:p.Asp197Val
NM_001374788.1:c.122A>T	NP_001361717.1:p.Asp41Val
NR_164663.1:n.292A>T