Canonical Allele Identifier: CA352134303
Gene: MYD88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38141151G>T , CM000665.2:g.38141151G>T GRCh38
NC_000003.11:g.38182642G>T , CM000665.1:g.38182642G>T GRCh37
NC_000003.10:g.38157646G>T NCBI36
NG_016964.1:g.7674G>T , LRG_157:g.7674G>T
NG_023225.1:g.1092C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000463956.2:n.543G>T
ENST00000484513.2:n.2234G>T
ENST00000699084.1:n.1845G>T
ENST00000699085.1:n.1621G>T
ENST00000699086.1:c.537G>T
ENST00000396334.8:c.756G>T ENSP00000379625.4:p.Leu252=
ENST00000416282.3:n.859G>T
ENST00000417037.8:c.621G>T ENSP00000401399.4:p.Leu207=
ENST00000421516.3:c.780G>T ENSP00000391753.3:p.Leu260=
ENST00000650112.2:c.440G>T ENSP00000497991.2:p.Ter147Leu
ENST00000650905.2:c.756G>T MANE Select ENSP00000498360.2:p.Leu252=
ENST00000651800.2:c.575G>T ENSP00000499012.2:p.Ter192Leu
ENST00000652213.1:c.737G>T ENSP00000498576.1:p.Ter246Leu
ENST00000652590.1:n.984G>T
ENST00000396334.7:c.795G>T ENSP00000379625.3:p.Leu265=
ENST00000416282.2:n.859G>T
ENST00000417037.6:c.819G>T ENSP00000401399.2:p.Leu273=
ENST00000421516.1:c.816G>T ENSP00000391753.1:p.Leu272=
ENST00000424893.5:c.660G>T ENSP00000389979.1:p.Leu220=
ENST00000443433.6:c.614G>T ENSP00000390565.2:p.Ter205Leu
ENST00000463956.1:n.469G>T
ENST00000481122.5:n.549G>T
ENST00000484513.1:n.1446G>T
ENST00000495303.5:c.479G>T ENSP00000417848.1:p.Ter160Leu
NM_001172566.1:c.479G>T NP_001166037.1:p.Ter160Leu
NM_001172567.1:c.819G>T , LRG_157t1:c.819G>T NP_001166038.1:p.Leu273=
NM_001172568.1:c.660G>T NP_001166039.1:p.Leu220=
NM_001172569.1:c.614G>T NP_001166040.1:p.Ter205Leu
NM_002468.4:c.795G>T NP_002459.2:p.Leu265=
XM_005265172.1:c.776G>T XP_005265229.1:p.Ter259Leu
XM_006713170.1:c.641G>T XP_006713233.1:p.Ter214Leu
NM_001172566.2:c.440G>T NP_001166037.2:p.Ter147Leu
NM_001172567.2:c.780G>T NP_001166038.2:p.Leu260=
NM_001172568.2:c.621G>T NP_001166039.2:p.Leu207=
NM_001172569.2:c.575G>T NP_001166040.2:p.Ter192Leu
NM_001365876.1:c.737G>T NP_001352805.1:p.Ter246Leu
NM_001365877.1:c.602G>T NP_001352806.1:p.Ter201Leu
NM_002468.5:c.756G>T MANE Select NP_002459.3:p.Leu252=
NM_001172569.3:c.575G>T NP_001166040.2:p.Ter192Leu
NM_001374787.1:c.713G>T NP_001361716.1:p.Ter238Leu
NM_001374788.1:c.288G>T NP_001361717.1:p.Leu96=
NR_164663.1:n.439G>T