Canonical Allele Identifier: CA352132865

Gene: MYD88

Linked Data

• dbSNP Id: rs1701052125
• MyVariant Identifiers: chr3:g.38182014C>G (hg19) ; chr3:g.38140523C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.386C>G
ENST00000484513.2:n.1889C>G
ENST00000699084.1:n.1500C>G
ENST00000699085.1:n.1464C>G
ENST00000699086.1:c.399C>G
ENST00000396334.8:c.599C>G	ENSP00000379625.4:p.Pro200Arg
ENST00000416282.3:n.514C>G
ENST00000417037.8:c.464C>G	ENSP00000401399.4:p.Pro155Arg
ENST00000421516.3:c.599C>G	ENSP00000391753.3:p.Pro200Arg
ENST00000650112.2:c.329-234C>G	ENSP00000497991.2:n.329-234C>G
ENST00000650905.2:c.599C>G MANE Select	ENSP00000498360.2:p.Pro200Arg
ENST00000651800.2:c.464-234C>G	ENSP00000499012.2:n.464-234C>G
ENST00000652213.1:c.599C>G	ENSP00000498576.1:p.Pro200Arg
ENST00000652590.1:n.639C>G
ENST00000396334.7:c.638C>G	ENSP00000379625.3:p.Pro213Arg
ENST00000416282.2:n.514C>G
ENST00000417037.6:c.638C>G	ENSP00000401399.2:p.Pro213Arg
ENST00000421516.1:c.635C>G	ENSP00000391753.1:p.Pro212Arg
ENST00000424893.5:c.503C>G	ENSP00000389979.1:p.Pro168Arg
ENST00000443433.6:c.503-234C>G	ENSP00000390565.2:n.503-234C>G
ENST00000460295.1:n.1032C>G
ENST00000463956.1:n.312C>G
ENST00000481122.5:n.392C>G
ENST00000484513.1:n.1101C>G
ENST00000495303.5:c.368-234C>G	ENSP00000417848.1:n.368-234C>G
NM_001172566.1:c.368-234C>G	NP_001166037.1:n.368-234C>G
NM_001172567.1:c.638C>G , LRG_157t1:c.638C>G	NP_001166038.1:p.Pro213Arg
NM_001172568.1:c.503C>G	NP_001166039.1:p.Pro168Arg
NM_001172569.1:c.503-234C>G	NP_001166040.1:n.503-234C>G
NM_002468.4:c.638C>G	NP_002459.2:p.Pro213Arg
XM_005265172.1:c.638C>G	XP_005265229.1:p.Pro213Arg
XM_006713170.1:c.503C>G	XP_006713233.1:p.Pro168Arg
NM_001172566.2:c.329-234C>G	NP_001166037.2:n.329-234C>G
NM_001172567.2:c.599C>G	NP_001166038.2:p.Pro200Arg
NM_001172568.2:c.464C>G	NP_001166039.2:p.Pro155Arg
NM_001172569.2:c.464-234C>G	NP_001166040.2:n.464-234C>G
NM_001365876.1:c.599C>G	NP_001352805.1:p.Pro200Arg
NM_001365877.1:c.464C>G	NP_001352806.1:p.Pro155Arg
NM_002468.5:c.599C>G MANE Select	NP_002459.3:p.Pro200Arg
NM_001172569.3:c.464-234C>G	NP_001166040.2:n.464-234C>G
NM_001374787.1:c.599C>G	NP_001361716.1:p.Pro200Arg
NM_001374788.1:c.131C>G	NP_001361717.1:p.Pro44Arg
NR_164663.1:n.301C>G