Canonical Allele Identifier: CA402572328
Gene: MALT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58681304A>G , CM000680.2:g.58681304A>G GRCh38
NC_000018.9:g.56348536A>G , CM000680.1:g.56348536A>G GRCh37
NC_000018.8:g.54499516A>G NCBI36
NG_033893.1:g.14919A>G
NG_033893.2:g.14919A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697044.1:n.357A>G
ENST00000697098.1:n.87A>G
ENST00000648670.1:c.134A>G ENSP00000497173.1:p.His45Arg
ENST00000649217.2:c.344A>G MANE Select ENSP00000497997.1:p.His115Arg
ENST00000650045.1:c.344A>G ENSP00000497036.1:p.His115Arg
ENST00000345724.7:c.344A>G ENSP00000304161.3:p.His115Arg
ENST00000348428.7:c.344A>G ENSP00000319279.4:p.His115Arg
ENST00000591792.1:c.59A>G ENSP00000467222.1:p.His20Arg
NM_006785.3:c.344A>G NP_006776.1:p.His115Arg
NM_173844.2:c.344A>G NP_776216.1:p.His115Arg
XM_011525794.1:c.344A>G XP_011524096.1:p.His115Arg
XR_935190.1:n.568A>G
XR_935536.1:n.860-728T>C
XR_935537.1:n.860-728T>C
XR_935538.1:n.169-728T>C
NM_006785.4:c.344A>G MANE Select NP_006776.1:p.His115Arg
XR_001753134.1:n.568A>G
XR_001753135.1:n.568A>G
XR_001753136.1:n.568A>G
XR_935536.3:n.930-728T>C
XR_935537.2:n.930-728T>C
NM_173844.3:c.344A>G NP_776216.1:p.His115Arg