Canonical Allele Identifier: CA352132862

Gene: MYD88

Linked Data

• dbSNP Id: rs2125778756
• gnomAD v4: 3-38140522-C-G
• MyVariant Identifiers: chr3:g.38182013C>G (hg19) ; chr3:g.38140522C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38140522C>G , CM000665.2:g.38140522C>G	GRCh38
NC_000003.11:g.38182013C>G , CM000665.1:g.38182013C>G	GRCh37
NC_000003.10:g.38157017C>G	NCBI36
NG_016964.1:g.7045C>G , LRG_157:g.7045C>G
NG_023225.1:g.1721G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463956.2:n.385C>G
ENST00000484513.2:n.1888C>G
ENST00000699084.1:n.1499C>G
ENST00000699085.1:n.1463C>G
ENST00000699086.1:c.398C>G
ENST00000396334.8:c.598C>G	ENSP00000379625.4:p.Pro200Ala
ENST00000416282.3:n.513C>G
ENST00000417037.8:c.463C>G	ENSP00000401399.4:p.Pro155Ala
ENST00000421516.3:c.598C>G	ENSP00000391753.3:p.Pro200Ala
ENST00000650112.2:c.329-235C>G	ENSP00000497991.2:n.329-235C>G
ENST00000650905.2:c.598C>G MANE Select	ENSP00000498360.2:p.Pro200Ala
ENST00000651800.2:c.464-235C>G	ENSP00000499012.2:n.464-235C>G
ENST00000652213.1:c.598C>G	ENSP00000498576.1:p.Pro200Ala
ENST00000652590.1:n.638C>G
ENST00000396334.7:c.637C>G	ENSP00000379625.3:p.Pro213Ala
ENST00000416282.2:n.513C>G
ENST00000417037.6:c.637C>G	ENSP00000401399.2:p.Pro213Ala
ENST00000421516.1:c.634C>G	ENSP00000391753.1:p.Pro212Ala
ENST00000424893.5:c.502C>G	ENSP00000389979.1:p.Pro168Ala
ENST00000443433.6:c.503-235C>G	ENSP00000390565.2:n.503-235C>G
ENST00000460295.1:n.1031C>G
ENST00000463956.1:n.311C>G
ENST00000481122.5:n.391C>G
ENST00000484513.1:n.1100C>G
ENST00000495303.5:c.368-235C>G	ENSP00000417848.1:n.368-235C>G
NM_001172566.1:c.368-235C>G	NP_001166037.1:n.368-235C>G
NM_001172567.1:c.637C>G , LRG_157t1:c.637C>G	NP_001166038.1:p.Pro213Ala
NM_001172568.1:c.502C>G	NP_001166039.1:p.Pro168Ala
NM_001172569.1:c.503-235C>G	NP_001166040.1:n.503-235C>G
NM_002468.4:c.637C>G	NP_002459.2:p.Pro213Ala
XM_005265172.1:c.637C>G	XP_005265229.1:p.Pro213Ala
XM_006713170.1:c.502C>G	XP_006713233.1:p.Pro168Ala
NM_001172566.2:c.329-235C>G	NP_001166037.2:n.329-235C>G
NM_001172567.2:c.598C>G	NP_001166038.2:p.Pro200Ala
NM_001172568.2:c.463C>G	NP_001166039.2:p.Pro155Ala
NM_001172569.2:c.464-235C>G	NP_001166040.2:n.464-235C>G
NM_001365876.1:c.598C>G	NP_001352805.1:p.Pro200Ala
NM_001365877.1:c.463C>G	NP_001352806.1:p.Pro155Ala
NM_002468.5:c.598C>G MANE Select	NP_002459.3:p.Pro200Ala
NM_001172569.3:c.464-235C>G	NP_001166040.2:n.464-235C>G
NM_001374787.1:c.598C>G	NP_001361716.1:p.Pro200Ala
NM_001374788.1:c.130C>G	NP_001361717.1:p.Pro44Ala
NR_164663.1:n.300C>G