Canonical Allele Identifier: CA504043807

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58696415G>A , CM000680.2:g.58696415G>A	GRCh38
NC_000018.9:g.56363647G>A , CM000680.1:g.56363647G>A	GRCh37
NC_000018.8:g.54514627G>A	NCBI36
NG_033893.1:g.30030G>A
NG_033893.2:g.30030G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697044.1:n.439G>A
ENST00000697098.1:n.169G>A
ENST00000697099.1:n.34G>A
ENST00000648670.1:c.216G>A	ENSP00000497173.1:p.Gln72=
ENST00000649202.1:n.63G>A
ENST00000649217.2:c.426G>A MANE Select	ENSP00000497997.1:p.Gln142=
ENST00000650045.1:c.426G>A	ENSP00000497036.1:p.Gln142=
ENST00000345724.7:c.426G>A	ENSP00000304161.3:p.Gln142=
ENST00000348428.7:c.426G>A	ENSP00000319279.4:p.Gln142=
ENST00000591792.1:c.141G>A	ENSP00000467222.1:p.Gln47=
NM_006785.3:c.426G>A	NP_006776.1:p.Gln142=
NM_173844.2:c.426G>A	NP_776216.1:p.Gln142=
XM_011525794.1:c.426G>A	XP_011524096.1:p.Gln142=
XR_935190.1:n.650G>A
XR_935536.1:n.859+762C>T
XR_935537.1:n.859+762C>T
XR_935538.1:n.168+762C>T
NM_006785.4:c.426G>A MANE Select	NP_006776.1:p.Gln142=
XR_001753134.1:n.650G>A
XR_001753135.1:n.650G>A
XR_001753136.1:n.650G>A
XR_935536.3:n.929+762C>T
XR_935537.2:n.929+762C>T
NM_173844.3:c.426G>A	NP_776216.1:p.Gln142=