Canonical Allele Identifier: CA433330217

Gene: MYD88

Linked Data

• dbSNP Id: rs2125778749
• MyVariant Identifiers: chr3:g.38182012G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38140521G>C , CM000665.2:g.38140521G>C	GRCh38
NC_000003.11:g.38182012G>C , CM000665.1:g.38182012G>C	GRCh37
NC_000003.10:g.38157016G>C	NCBI36
NG_016964.1:g.7044G>C , LRG_157:g.7044G>C
NG_023225.1:g.1722C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463956.2:n.384G>C
ENST00000484513.2:n.1887G>C
ENST00000699084.1:n.1498G>C
ENST00000699085.1:n.1462G>C
ENST00000699086.1:c.397G>C
ENST00000396334.8:c.597G>C	ENSP00000379625.4:p.Leu199=
ENST00000416282.3:n.512G>C
ENST00000417037.8:c.462G>C	ENSP00000401399.4:p.Leu154=
ENST00000421516.3:c.597G>C	ENSP00000391753.3:p.Leu199=
ENST00000650112.2:c.329-236G>C	ENSP00000497991.2:n.329-236G>C
ENST00000650905.2:c.597G>C MANE Select	ENSP00000498360.2:p.Leu199=
ENST00000651800.2:c.464-236G>C	ENSP00000499012.2:n.464-236G>C
ENST00000652213.1:c.597G>C	ENSP00000498576.1:p.Leu199=
ENST00000652590.1:n.637G>C
ENST00000396334.7:c.636G>C	ENSP00000379625.3:p.Leu212=
ENST00000416282.2:n.512G>C
ENST00000417037.6:c.636G>C	ENSP00000401399.2:p.Leu212=
ENST00000421516.1:c.633G>C	ENSP00000391753.1:p.Leu211=
ENST00000424893.5:c.501G>C	ENSP00000389979.1:p.Leu167=
ENST00000443433.6:c.503-236G>C	ENSP00000390565.2:n.503-236G>C
ENST00000460295.1:n.1030G>C
ENST00000463956.1:n.310G>C
ENST00000481122.5:n.390G>C
ENST00000484513.1:n.1099G>C
ENST00000495303.5:c.368-236G>C	ENSP00000417848.1:n.368-236G>C
NM_001172566.1:c.368-236G>C	NP_001166037.1:n.368-236G>C
NM_001172567.1:c.636G>C , LRG_157t1:c.636G>C	NP_001166038.1:p.Leu212=
NM_001172568.1:c.501G>C	NP_001166039.1:p.Leu167=
NM_001172569.1:c.503-236G>C	NP_001166040.1:n.503-236G>C
NM_002468.4:c.636G>C	NP_002459.2:p.Leu212=
XM_005265172.1:c.636G>C	XP_005265229.1:p.Leu212=
XM_006713170.1:c.501G>C	XP_006713233.1:p.Leu167=
NM_001172566.2:c.329-236G>C	NP_001166037.2:n.329-236G>C
NM_001172567.2:c.597G>C	NP_001166038.2:p.Leu199=
NM_001172568.2:c.462G>C	NP_001166039.2:p.Leu154=
NM_001172569.2:c.464-236G>C	NP_001166040.2:n.464-236G>C
NM_001365876.1:c.597G>C	NP_001352805.1:p.Leu199=
NM_001365877.1:c.462G>C	NP_001352806.1:p.Leu154=
NM_002468.5:c.597G>C MANE Select	NP_002459.3:p.Leu199=
NM_001172569.3:c.464-236G>C	NP_001166040.2:n.464-236G>C
NM_001374787.1:c.597G>C	NP_001361716.1:p.Leu199=
NM_001374788.1:c.129G>C	NP_001361717.1:p.Leu43=
NR_164663.1:n.299G>C