Canonical Allele Identifier: CA1358376235
Gene: MYD88 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.38140523C= , CM000665.2:g.38140523C= GRCh38
NC_000003.11:g.38182014C= , CM000665.1:g.38182014C= GRCh37
NC_000003.10:g.38157018C= NCBI36
NG_016964.1:g.7046C= , LRG_157:g.7046C=
NG_023225.1:g.1720G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463956.2:n.386C=
ENST00000484513.2:n.1889C=
ENST00000699084.1:n.1500C=
ENST00000699085.1:n.1464C=
ENST00000699086.1:c.399C=
ENST00000396334.8:c.599C= ENSP00000379625.4:p.Pro200=
ENST00000416282.3:n.514C=
ENST00000417037.8:c.464C= ENSP00000401399.4:p.Pro155=
ENST00000421516.3:c.599C= ENSP00000391753.3:p.Pro200=
ENST00000650112.2:c.329-234C= ENSP00000497991.2:n.329-234C=
ENST00000650905.2:c.599C= MANE Select ENSP00000498360.2:p.Pro200=
ENST00000651800.2:c.464-234C= ENSP00000499012.2:n.464-234C=
ENST00000652213.1:c.599C= ENSP00000498576.1:p.Pro200=
ENST00000652590.1:n.639C=
ENST00000396334.7:c.638C= ENSP00000379625.3:p.Pro213=
ENST00000416282.2:n.514C=
ENST00000417037.6:c.638C= ENSP00000401399.2:p.Pro213=
ENST00000421516.1:c.635C= ENSP00000391753.1:p.Pro212=
ENST00000424893.5:c.503C= ENSP00000389979.1:p.Pro168=
ENST00000443433.6:c.503-234C= ENSP00000390565.2:n.503-234C=
ENST00000460295.1:n.1032C=
ENST00000463956.1:n.312C=
ENST00000481122.5:n.392C=
ENST00000484513.1:n.1101C=
ENST00000495303.5:c.368-234C= ENSP00000417848.1:n.368-234C=
NM_001172566.1:c.368-234C= NP_001166037.1:n.368-234C=
NM_001172567.1:c.638C= , LRG_157t1:c.638C= NP_001166038.1:p.Pro213=
NM_001172568.1:c.503C= NP_001166039.1:p.Pro168=
NM_001172569.1:c.503-234C= NP_001166040.1:n.503-234C=
NM_002468.4:c.638C= NP_002459.2:p.Pro213=
XM_005265172.1:c.638C= XP_005265229.1:p.Pro213=
XM_006713170.1:c.503C= XP_006713233.1:p.Pro168=
NM_001172566.2:c.329-234C= NP_001166037.2:n.329-234C=
NM_001172567.2:c.599C= NP_001166038.2:p.Pro200=
NM_001172568.2:c.464C= NP_001166039.2:p.Pro155=
NM_001172569.2:c.464-234C= NP_001166040.2:n.464-234C=
NM_001365876.1:c.599C= NP_001352805.1:p.Pro200=
NM_001365877.1:c.464C= NP_001352806.1:p.Pro155=
NM_002468.5:c.599C= MANE Select NP_002459.3:p.Pro200=
NM_001172569.3:c.464-234C= NP_001166040.2:n.464-234C=
NM_001374787.1:c.599C= NP_001361716.1:p.Pro200=
NM_001374788.1:c.131C= NP_001361717.1:p.Pro44=
NR_164663.1:n.301C=