Canonical Allele Identifier: CA8977642

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58696435G>A , CM000680.2:g.58696435G>A	GRCh38
NC_000018.9:g.56363667G>A , CM000680.1:g.56363667G>A	GRCh37
NC_000018.8:g.54514647G>A	NCBI36
NG_033893.1:g.30050G>A
NG_033893.2:g.30050G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697044.1:n.459G>A
ENST00000697098.1:n.189G>A
ENST00000697099.1:n.54G>A
ENST00000648670.1:c.236G>A	ENSP00000497173.1:p.Arg79Gln
ENST00000649202.1:n.83G>A
ENST00000649217.2:c.446G>A MANE Select	ENSP00000497997.1:p.Arg149Gln
ENST00000650045.1:c.446G>A	ENSP00000497036.1:p.Arg149Gln
ENST00000345724.7:c.446G>A	ENSP00000304161.3:p.Arg149Gln
ENST00000348428.7:c.446G>A	ENSP00000319279.4:p.Arg149Gln
ENST00000591792.1:c.161G>A	ENSP00000467222.1:p.Arg54Gln
NM_006785.3:c.446G>A	NP_006776.1:p.Arg149Gln
NM_173844.2:c.446G>A	NP_776216.1:p.Arg149Gln
XM_011525794.1:c.446G>A	XP_011524096.1:p.Arg149Gln
XR_935190.1:n.670G>A
XR_935536.1:n.859+742C>T
XR_935537.1:n.859+742C>T
XR_935538.1:n.168+742C>T
NM_006785.4:c.446G>A MANE Select	NP_006776.1:p.Arg149Gln
XR_001753134.1:n.670G>A
XR_001753135.1:n.670G>A
XR_001753136.1:n.670G>A
XR_935536.3:n.929+742C>T
XR_935537.2:n.929+742C>T
NM_173844.3:c.446G>A	NP_776216.1:p.Arg149Gln