Canonical Allele Identifier: CA1358376422
Gene: MYD88 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38140988A= , CM000665.2:g.38140988A= GRCh38
NC_000003.11:g.38182479A= , CM000665.1:g.38182479A= GRCh37
NC_000003.10:g.38157483A= NCBI36
NG_016964.1:g.7511A= , LRG_157:g.7511A=
NG_023225.1:g.1255T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463956.2:n.523+140A=
ENST00000484513.2:n.2214+140A=
ENST00000699084.1:n.1825+140A=
ENST00000699085.1:n.1601+140A=
ENST00000699086.1:c.517+140A=
ENST00000396334.8:c.736+140A= ENSP00000379625.4:n.736+140A=
ENST00000416282.3:n.839+140A=
ENST00000417037.8:c.601+140A= ENSP00000401399.4:n.601+140A=
ENST00000421516.3:c.760+140A= ENSP00000391753.3:n.760+140A=
ENST00000650112.2:c.420+140A= ENSP00000497991.2:n.420+140A=
ENST00000650905.2:c.736+140A= MANE Select ENSP00000498360.2:n.736+140A=
ENST00000651800.2:c.555+140A= ENSP00000499012.2:n.555+140A=
ENST00000652213.1:c.717+140A= ENSP00000498576.1:n.717+140A=
ENST00000652590.1:n.964+140A=
ENST00000396334.7:c.775+140A= ENSP00000379625.3:n.775+140A=
ENST00000416282.2:n.839+140A=
ENST00000417037.6:c.799+140A= ENSP00000401399.2:n.799+140A=
ENST00000421516.1:c.796+140A= ENSP00000391753.1:n.796+140A=
ENST00000424893.5:c.640+140A= ENSP00000389979.1:n.640+140A=
ENST00000443433.6:c.594+140A= ENSP00000390565.2:n.594+140A=
ENST00000463956.1:n.449+140A=
ENST00000481122.5:n.529+140A=
ENST00000484513.1:n.1426+140A=
ENST00000495303.5:c.459+140A= ENSP00000417848.1:n.459+140A=
NM_001172566.1:c.459+140A= NP_001166037.1:n.459+140A=
NM_001172567.1:c.799+140A= , LRG_157t1:c.799+140A= NP_001166038.1:n.799+140A=
NM_001172568.1:c.640+140A= NP_001166039.1:n.640+140A=
NM_001172569.1:c.594+140A= NP_001166040.1:n.594+140A=
NM_002468.4:c.775+140A= NP_002459.2:n.775+140A=
XM_005265172.1:c.756+140A= XP_005265229.1:n.756+140A=
XM_006713170.1:c.621+140A= XP_006713233.1:n.621+140A=
NM_001172566.2:c.420+140A= NP_001166037.2:n.420+140A=
NM_001172567.2:c.760+140A= NP_001166038.2:n.760+140A=
NM_001172568.2:c.601+140A= NP_001166039.2:n.601+140A=
NM_001172569.2:c.555+140A= NP_001166040.2:n.555+140A=
NM_001365876.1:c.717+140A= NP_001352805.1:n.717+140A=
NM_001365877.1:c.582+140A= NP_001352806.1:n.582+140A=
NM_002468.5:c.736+140A= MANE Select NP_002459.3:n.736+140A=
NM_001172569.3:c.555+140A= NP_001166040.2:n.555+140A=
NM_001374787.1:c.693+140A= NP_001361716.1:n.693+140A=
NM_001374788.1:c.268+140A= NP_001361717.1:n.268+140A=
NR_164663.1:n.419+140A=