Canonical Allele Identifier: CA1358376478
Gene: MYD88 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38141123G= , CM000665.2:g.38141123G= GRCh38
NC_000003.11:g.38182614G= , CM000665.1:g.38182614G= GRCh37
NC_000003.10:g.38157618G= NCBI36
NG_016964.1:g.7646G= , LRG_157:g.7646G=
NG_023225.1:g.1120C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463956.2:n.524-9G=
ENST00000484513.2:n.2215-9G=
ENST00000699084.1:n.1826-9G=
ENST00000699085.1:n.1602-9G=
ENST00000699086.1:c.518-9G=
ENST00000396334.8:c.737-9G= ENSP00000379625.4:n.737-9G=
ENST00000416282.3:n.840-9G=
ENST00000417037.8:c.602-9G= ENSP00000401399.4:n.602-9G=
ENST00000421516.3:c.761-9G= ENSP00000391753.3:n.761-9G=
ENST00000650112.2:c.421-9G= ENSP00000497991.2:n.421-9G=
ENST00000650905.2:c.737-9G= MANE Select ENSP00000498360.2:n.737-9G=
ENST00000651800.2:c.556-9G= ENSP00000499012.2:n.556-9G=
ENST00000652213.1:c.718-9G= ENSP00000498576.1:n.718-9G=
ENST00000652590.1:n.965-9G=
ENST00000396334.7:c.776-9G= ENSP00000379625.3:n.776-9G=
ENST00000416282.2:n.840-9G=
ENST00000417037.6:c.800-9G= ENSP00000401399.2:n.800-9G=
ENST00000421516.1:c.797-9G= ENSP00000391753.1:n.797-9G=
ENST00000424893.5:c.641-9G= ENSP00000389979.1:n.641-9G=
ENST00000443433.6:c.595-9G= ENSP00000390565.2:n.595-9G=
ENST00000463956.1:n.450-9G=
ENST00000481122.5:n.530-9G=
ENST00000484513.1:n.1427-9G=
ENST00000495303.5:c.460-9G= ENSP00000417848.1:n.460-9G=
NM_001172566.1:c.460-9G= NP_001166037.1:n.460-9G=
NM_001172567.1:c.800-9G= , LRG_157t1:c.800-9G= NP_001166038.1:n.800-9G=
NM_001172568.1:c.641-9G= NP_001166039.1:n.641-9G=
NM_001172569.1:c.595-9G= NP_001166040.1:n.595-9G=
NM_002468.4:c.776-9G= NP_002459.2:n.776-9G=
XM_005265172.1:c.757-9G= XP_005265229.1:n.757-9G=
XM_006713170.1:c.622-9G= XP_006713233.1:n.622-9G=
NM_001172566.2:c.421-9G= NP_001166037.2:n.421-9G=
NM_001172567.2:c.761-9G= NP_001166038.2:n.761-9G=
NM_001172568.2:c.602-9G= NP_001166039.2:n.602-9G=
NM_001172569.2:c.556-9G= NP_001166040.2:n.556-9G=
NM_001365876.1:c.718-9G= NP_001352805.1:n.718-9G=
NM_001365877.1:c.583-9G= NP_001352806.1:n.583-9G=
NM_002468.5:c.737-9G= MANE Select NP_002459.3:n.737-9G=
NM_001172569.3:c.556-9G= NP_001166040.2:n.556-9G=
NM_001374787.1:c.694-9G= NP_001361716.1:n.694-9G=
NM_001374788.1:c.269-9G= NP_001361717.1:n.269-9G=
NR_164663.1:n.420-9G=