Canonical Allele Identifier: CA402574482
Gene: MALT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58733414G>A , CM000680.2:g.58733414G>A GRCh38
NC_000018.9:g.56400646G>A , CM000680.1:g.56400646G>A GRCh37
NC_000018.8:g.54551626G>A NCBI36
NG_033893.1:g.67029G>A
NG_033893.2:g.67029G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697045.1:n.1094G>A
ENST00000697046.1:n.392G>A
ENST00000697098.1:n.983G>A
ENST00000697099.1:n.848G>A
ENST00000648670.1:c.894G>A ENSP00000497173.1:n.894G>A
ENST00000649125.1:n.1109G>A
ENST00000649202.1:n.844G>A
ENST00000649217.2:c.1240G>A MANE Select ENSP00000497997.1:p.Gly414Arg
ENST00000650045.1:c.1240G>A ENSP00000497036.1:p.Gly414Arg
ENST00000345724.7:c.1207G>A ENSP00000304161.3:p.Gly403Arg
ENST00000348428.7:c.1240G>A ENSP00000319279.4:p.Gly414Arg
NM_006785.3:c.1240G>A NP_006776.1:p.Gly414Arg
NM_173844.2:c.1207G>A NP_776216.1:p.Gly403Arg
XM_011525794.1:c.*20G>A XP_011524096.1:n.*20G>A
XR_935190.1:n.1464G>A
XR_935538.1:n.78-36147C>T
NM_006785.4:c.1240G>A MANE Select NP_006776.1:p.Gly414Arg
XR_001753134.1:n.1464G>A
XR_001753135.1:n.1431G>A
XR_001753136.1:n.1464G>A
NM_173844.3:c.1207G>A NP_776216.1:p.Gly403Arg