Canonical Allele Identifier: CA402572794
Gene: MALT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58700484A>G , CM000680.2:g.58700484A>G GRCh38
NC_000018.9:g.56367716A>G , CM000680.1:g.56367716A>G GRCh37
NC_000018.8:g.54518696A>G NCBI36
NG_033893.1:g.34099A>G
NG_033893.2:g.34099A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697044.1:n.555A>G
ENST00000697098.1:n.285A>G
ENST00000697099.1:n.150A>G
ENST00000648670.1:c.332A>G ENSP00000497173.1:p.His111Arg
ENST00000649202.1:n.179A>G
ENST00000649217.2:c.542A>G MANE Select ENSP00000497997.1:p.His181Arg
ENST00000650045.1:c.542A>G ENSP00000497036.1:p.His181Arg
ENST00000345724.7:c.542A>G ENSP00000304161.3:p.His181Arg
ENST00000348428.7:c.542A>G ENSP00000319279.4:p.His181Arg
ENST00000591792.1:c.257A>G ENSP00000467222.1:p.His86Arg
NM_006785.3:c.542A>G NP_006776.1:p.His181Arg
NM_173844.2:c.542A>G NP_776216.1:p.His181Arg
XM_011525794.1:c.542A>G XP_011524096.1:p.His181Arg
XR_935190.1:n.766A>G
XR_935538.1:n.78-3217T>C
NM_006785.4:c.542A>G MANE Select NP_006776.1:p.His181Arg
XR_001753134.1:n.766A>G
XR_001753135.1:n.766A>G
XR_001753136.1:n.766A>G
NM_173844.3:c.542A>G NP_776216.1:p.His181Arg