Canonical Allele Identifier: CA352134289

Gene: MYD88

Linked Data

• gnomAD v4: 3-38141148-A-C
• MyVariant Identifiers: chr3:g.38182639A>C (hg19) ; chr3:g.38141148A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38141148A>C , CM000665.2:g.38141148A>C	GRCh38
NC_000003.11:g.38182639A>C , CM000665.1:g.38182639A>C	GRCh37
NC_000003.10:g.38157643A>C	NCBI36
NG_016964.1:g.7671A>C , LRG_157:g.7671A>C
NG_023225.1:g.1095T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463956.2:n.540A>C
ENST00000484513.2:n.2231A>C
ENST00000699084.1:n.1842A>C
ENST00000699085.1:n.1618A>C
ENST00000699086.1:c.534A>C
ENST00000396334.8:c.753A>C	ENSP00000379625.4:p.Arg251=
ENST00000416282.3:n.856A>C
ENST00000417037.8:c.618A>C	ENSP00000401399.4:p.Arg206=
ENST00000421516.3:c.777A>C	ENSP00000391753.3:p.Arg259=
ENST00000650112.2:c.437A>C	ENSP00000497991.2:p.Asp146Ala
ENST00000650905.2:c.753A>C MANE Select	ENSP00000498360.2:p.Arg251=
ENST00000651800.2:c.572A>C	ENSP00000499012.2:p.Asp191Ala
ENST00000652213.1:c.734A>C	ENSP00000498576.1:p.Asp245Ala
ENST00000652590.1:n.981A>C
ENST00000396334.7:c.792A>C	ENSP00000379625.3:p.Arg264=
ENST00000416282.2:n.856A>C
ENST00000417037.6:c.816A>C	ENSP00000401399.2:p.Arg272=
ENST00000421516.1:c.813A>C	ENSP00000391753.1:p.Arg271=
ENST00000424893.5:c.657A>C	ENSP00000389979.1:p.Arg219=
ENST00000443433.6:c.611A>C	ENSP00000390565.2:p.Asp204Ala
ENST00000463956.1:n.466A>C
ENST00000481122.5:n.546A>C
ENST00000484513.1:n.1443A>C
ENST00000495303.5:c.476A>C	ENSP00000417848.1:p.Asp159Ala
NM_001172566.1:c.476A>C	NP_001166037.1:p.Asp159Ala
NM_001172567.1:c.816A>C , LRG_157t1:c.816A>C	NP_001166038.1:p.Arg272=
NM_001172568.1:c.657A>C	NP_001166039.1:p.Arg219=
NM_001172569.1:c.611A>C	NP_001166040.1:p.Asp204Ala
NM_002468.4:c.792A>C	NP_002459.2:p.Arg264=
XM_005265172.1:c.773A>C	XP_005265229.1:p.Asp258Ala
XM_006713170.1:c.638A>C	XP_006713233.1:p.Asp213Ala
NM_001172566.2:c.437A>C	NP_001166037.2:p.Asp146Ala
NM_001172567.2:c.777A>C	NP_001166038.2:p.Arg259=
NM_001172568.2:c.618A>C	NP_001166039.2:p.Arg206=
NM_001172569.2:c.572A>C	NP_001166040.2:p.Asp191Ala
NM_001365876.1:c.734A>C	NP_001352805.1:p.Asp245Ala
NM_001365877.1:c.599A>C	NP_001352806.1:p.Asp200Ala
NM_002468.5:c.753A>C MANE Select	NP_002459.3:p.Arg251=
NM_001172569.3:c.572A>C	NP_001166040.2:p.Asp191Ala
NM_001374787.1:c.710A>C	NP_001361716.1:p.Asp237Ala
NM_001374788.1:c.285A>C	NP_001361717.1:p.Arg95=
NR_164663.1:n.436A>C