Canonical Allele Identifier: CA2665071941

Gene: MYD88

Linked Data

• gnomAD v4: 3-38140978-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38140978G>T , CM000665.2:g.38140978G>T	GRCh38
NC_000003.11:g.38182469G>T , CM000665.1:g.38182469G>T	GRCh37
NC_000003.10:g.38157473G>T	NCBI36
NG_016964.1:g.7501G>T , LRG_157:g.7501G>T
NG_023225.1:g.1265C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463956.2:n.523+130G>T
ENST00000484513.2:n.2214+130G>T
ENST00000699084.1:n.1825+130G>T
ENST00000699085.1:n.1601+130G>T
ENST00000699086.1:c.517+130G>T
ENST00000396334.8:c.736+130G>T	ENSP00000379625.4:n.736+130G>T
ENST00000416282.3:n.839+130G>T
ENST00000417037.8:c.601+130G>T	ENSP00000401399.4:n.601+130G>T
ENST00000421516.3:c.760+130G>T	ENSP00000391753.3:n.760+130G>T
ENST00000650112.2:c.420+130G>T	ENSP00000497991.2:n.420+130G>T
ENST00000650905.2:c.736+130G>T MANE Select	ENSP00000498360.2:n.736+130G>T
ENST00000651800.2:c.555+130G>T	ENSP00000499012.2:n.555+130G>T
ENST00000652213.1:c.717+130G>T	ENSP00000498576.1:n.717+130G>T
ENST00000652590.1:n.964+130G>T
ENST00000396334.7:c.775+130G>T	ENSP00000379625.3:n.775+130G>T
ENST00000416282.2:n.839+130G>T
ENST00000417037.6:c.799+130G>T	ENSP00000401399.2:n.799+130G>T
ENST00000421516.1:c.796+130G>T	ENSP00000391753.1:n.796+130G>T
ENST00000424893.5:c.640+130G>T	ENSP00000389979.1:n.640+130G>T
ENST00000443433.6:c.594+130G>T	ENSP00000390565.2:n.594+130G>T
ENST00000463956.1:n.449+130G>T
ENST00000481122.5:n.529+130G>T
ENST00000484513.1:n.1426+130G>T
ENST00000495303.5:c.459+130G>T	ENSP00000417848.1:n.459+130G>T
NM_001172566.1:c.459+130G>T	NP_001166037.1:n.459+130G>T
NM_001172567.1:c.799+130G>T , LRG_157t1:c.799+130G>T	NP_001166038.1:n.799+130G>T
NM_001172568.1:c.640+130G>T	NP_001166039.1:n.640+130G>T
NM_001172569.1:c.594+130G>T	NP_001166040.1:n.594+130G>T
NM_002468.4:c.775+130G>T	NP_002459.2:n.775+130G>T
XM_005265172.1:c.756+130G>T	XP_005265229.1:n.756+130G>T
XM_006713170.1:c.621+130G>T	XP_006713233.1:n.621+130G>T
NM_001172566.2:c.420+130G>T	NP_001166037.2:n.420+130G>T
NM_001172567.2:c.760+130G>T	NP_001166038.2:n.760+130G>T
NM_001172568.2:c.601+130G>T	NP_001166039.2:n.601+130G>T
NM_001172569.2:c.555+130G>T	NP_001166040.2:n.555+130G>T
NM_001365876.1:c.717+130G>T	NP_001352805.1:n.717+130G>T
NM_001365877.1:c.582+130G>T	NP_001352806.1:n.582+130G>T
NM_002468.5:c.736+130G>T MANE Select	NP_002459.3:n.736+130G>T
NM_001172569.3:c.555+130G>T	NP_001166040.2:n.555+130G>T
NM_001374787.1:c.693+130G>T	NP_001361716.1:n.693+130G>T
NM_001374788.1:c.268+130G>T	NP_001361717.1:n.268+130G>T
NR_164663.1:n.419+130G>T