Canonical Allele Identifier: CA402572414

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58696368A>G , CM000680.2:g.58696368A>G	GRCh38
NC_000018.9:g.56363600A>G , CM000680.1:g.56363600A>G	GRCh37
NC_000018.8:g.54514580A>G	NCBI36
NG_033893.1:g.29983A>G
NG_033893.2:g.29983A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697044.1:n.392A>G
ENST00000697098.1:n.122A>G
ENST00000648670.1:c.169A>G	ENSP00000497173.1:p.Ile57Val
ENST00000649202.1:n.16A>G
ENST00000649217.2:c.379A>G MANE Select	ENSP00000497997.1:p.Ile127Val
ENST00000650045.1:c.379A>G	ENSP00000497036.1:p.Ile127Val
ENST00000345724.7:c.379A>G	ENSP00000304161.3:p.Ile127Val
ENST00000348428.7:c.379A>G	ENSP00000319279.4:p.Ile127Val
ENST00000591792.1:c.94A>G	ENSP00000467222.1:p.Ile32Val
NM_006785.3:c.379A>G	NP_006776.1:p.Ile127Val
NM_173844.2:c.379A>G	NP_776216.1:p.Ile127Val
XM_011525794.1:c.379A>G	XP_011524096.1:p.Ile127Val
XR_935190.1:n.603A>G
XR_935536.1:n.859+809T>C
XR_935537.1:n.859+809T>C
XR_935538.1:n.168+809T>C
NM_006785.4:c.379A>G MANE Select	NP_006776.1:p.Ile127Val
XR_001753134.1:n.603A>G
XR_001753135.1:n.603A>G
XR_001753136.1:n.603A>G
XR_935536.3:n.929+809T>C
XR_935537.2:n.929+809T>C
NM_173844.3:c.379A>G	NP_776216.1:p.Ile127Val