Canonical Allele Identifier: CA8977674
Gene: MALT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58700591A>G , CM000680.2:g.58700591A>G GRCh38
NC_000018.9:g.56367823A>G , CM000680.1:g.56367823A>G GRCh37
NC_000018.8:g.54518803A>G NCBI36
NG_033893.1:g.34206A>G
NG_033893.2:g.34206A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697044.1:n.662A>G
ENST00000697098.1:n.392A>G
ENST00000697099.1:n.257A>G
ENST00000648670.1:c.439A>G ENSP00000497173.1:p.Ser147Gly
ENST00000649202.1:n.286A>G
ENST00000649217.2:c.649A>G MANE Select ENSP00000497997.1:p.Arg217Gly
ENST00000650045.1:c.649A>G ENSP00000497036.1:p.Arg217Gly
ENST00000345724.7:c.649A>G ENSP00000304161.3:p.Arg217Gly
ENST00000348428.7:c.649A>G ENSP00000319279.4:p.Arg217Gly
NM_006785.3:c.649A>G NP_006776.1:p.Arg217Gly
NM_173844.2:c.649A>G NP_776216.1:p.Arg217Gly
XM_011525794.1:c.649A>G XP_011524096.1:p.Arg217Gly
XR_935190.1:n.873A>G
XR_935538.1:n.78-3324T>C
NM_006785.4:c.649A>G MANE Select NP_006776.1:p.Arg217Gly
XR_001753134.1:n.873A>G
XR_001753135.1:n.873A>G
XR_001753136.1:n.873A>G
NM_173844.3:c.649A>G NP_776216.1:p.Arg217Gly