Canonical Allele Identifier: CA8977672
Gene: MALT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58700583G>T , CM000680.2:g.58700583G>T GRCh38
NC_000018.9:g.56367815G>T , CM000680.1:g.56367815G>T GRCh37
NC_000018.8:g.54518795G>T NCBI36
NG_033893.1:g.34198G>T
NG_033893.2:g.34198G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697044.1:n.654G>T
ENST00000697098.1:n.384G>T
ENST00000697099.1:n.249G>T
ENST00000648670.1:c.431G>T ENSP00000497173.1:p.Ser144Ile
ENST00000649202.1:n.278G>T
ENST00000649217.2:c.641G>T MANE Select ENSP00000497997.1:p.Ser214Ile
ENST00000650045.1:c.641G>T ENSP00000497036.1:p.Ser214Ile
ENST00000345724.7:c.641G>T ENSP00000304161.3:p.Ser214Ile
ENST00000348428.7:c.641G>T ENSP00000319279.4:p.Ser214Ile
ENST00000591792.1:c.356G>T ENSP00000467222.1:p.Ser119Ile
NM_006785.3:c.641G>T NP_006776.1:p.Ser214Ile
NM_173844.2:c.641G>T NP_776216.1:p.Ser214Ile
XM_011525794.1:c.641G>T XP_011524096.1:p.Ser214Ile
XR_935190.1:n.865G>T
XR_935538.1:n.78-3316C>A
NM_006785.4:c.641G>T MANE Select NP_006776.1:p.Ser214Ile
XR_001753134.1:n.865G>T
XR_001753135.1:n.865G>T
XR_001753136.1:n.865G>T
NM_173844.3:c.641G>T NP_776216.1:p.Ser214Ile