Canonical Allele Identifier: CA352134305

Gene: MYD88

Linked Data

• dbSNP Id: rs2125780307
• MyVariant Identifiers: chr3:g.38182643A>C (hg19) ; chr3:g.38141152A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38141152A>C , CM000665.2:g.38141152A>C	GRCh38
NC_000003.11:g.38182643A>C , CM000665.1:g.38182643A>C	GRCh37
NC_000003.10:g.38157647A>C	NCBI36
NG_016964.1:g.7675A>C , LRG_157:g.7675A>C
NG_023225.1:g.1091T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.544A>C
ENST00000484513.2:n.2235A>C
ENST00000699084.1:n.1846A>C
ENST00000699085.1:n.1622A>C
ENST00000699086.1:c.538A>C
ENST00000396334.8:c.757A>C	ENSP00000379625.4:p.Ile253Leu
ENST00000416282.3:n.860A>C
ENST00000417037.8:c.622A>C	ENSP00000401399.4:p.Ile208Leu
ENST00000421516.3:c.781A>C	ENSP00000391753.3:p.Ile261Leu
ENST00000650112.2:c.441A>C	ENSP00000497991.2:p.Ter147Cys
ENST00000650905.2:c.757A>C MANE Select	ENSP00000498360.2:p.Ile253Leu
ENST00000651800.2:c.576A>C	ENSP00000499012.2:p.Ter192Cys
ENST00000652213.1:c.738A>C	ENSP00000498576.1:p.Ter246Cys
ENST00000652590.1:n.985A>C
ENST00000396334.7:c.796A>C	ENSP00000379625.3:p.Ile266Leu
ENST00000416282.2:n.860A>C
ENST00000417037.6:c.820A>C	ENSP00000401399.2:p.Ile274Leu
ENST00000421516.1:c.817A>C	ENSP00000391753.1:p.Ile273Leu
ENST00000424893.5:c.661A>C	ENSP00000389979.1:p.Ile221Leu
ENST00000443433.6:c.615A>C	ENSP00000390565.2:p.Ter205Cys
ENST00000463956.1:n.470A>C
ENST00000481122.5:n.550A>C
ENST00000484513.1:n.1447A>C
ENST00000495303.5:c.480A>C	ENSP00000417848.1:p.Ter160Cys
NM_001172566.1:c.480A>C	NP_001166037.1:p.Ter160Cys
NM_001172567.1:c.820A>C , LRG_157t1:c.820A>C	NP_001166038.1:p.Ile274Leu
NM_001172568.1:c.661A>C	NP_001166039.1:p.Ile221Leu
NM_001172569.1:c.615A>C	NP_001166040.1:p.Ter205Cys
NM_002468.4:c.796A>C	NP_002459.2:p.Ile266Leu
XM_005265172.1:c.777A>C	XP_005265229.1:p.Ter259Cys
XM_006713170.1:c.642A>C	XP_006713233.1:p.Ter214Cys
NM_001172566.2:c.441A>C	NP_001166037.2:p.Ter147Cys
NM_001172567.2:c.781A>C	NP_001166038.2:p.Ile261Leu
NM_001172568.2:c.622A>C	NP_001166039.2:p.Ile208Leu
NM_001172569.2:c.576A>C	NP_001166040.2:p.Ter192Cys
NM_001365876.1:c.738A>C	NP_001352805.1:p.Ter246Cys
NM_001365877.1:c.603A>C	NP_001352806.1:p.Ter201Cys
NM_002468.5:c.757A>C MANE Select	NP_002459.3:p.Ile253Leu
NM_001172569.3:c.576A>C	NP_001166040.2:p.Ter192Cys
NM_001374787.1:c.714A>C	NP_001361716.1:p.Ter238Cys
NM_001374788.1:c.289A>C	NP_001361717.1:p.Ile97Leu
NR_164663.1:n.440A>C