Canonical Allele Identifier: CA402573416

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58709534A>G , CM000680.2:g.58709534A>G	GRCh38
NC_000018.9:g.56376766A>G , CM000680.1:g.56376766A>G	GRCh37
NC_000018.8:g.54527746A>G	NCBI36
NG_033893.1:g.43149A>G
NG_033893.2:g.43149A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697045.1:n.198A>G
ENST00000697098.1:n.549A>G
ENST00000697099.1:n.414A>G
ENST00000648670.1:c.440-442A>G	ENSP00000497173.1:n.440-442A>G
ENST00000649125.1:n.213A>G
ENST00000649202.1:n.443A>G
ENST00000649217.2:c.806A>G MANE Select	ENSP00000497997.1:p.His269Arg
ENST00000650045.1:c.806A>G	ENSP00000497036.1:p.His269Arg
ENST00000345724.7:c.806A>G	ENSP00000304161.3:p.His269Arg
ENST00000348428.7:c.806A>G	ENSP00000319279.4:p.His269Arg
NM_006785.3:c.806A>G	NP_006776.1:p.His269Arg
NM_173844.2:c.806A>G	NP_776216.1:p.His269Arg
XM_011525794.1:c.806A>G	XP_011524096.1:p.His269Arg
XR_935190.1:n.1030A>G
XR_935538.1:n.78-12267T>C
NM_006785.4:c.806A>G MANE Select	NP_006776.1:p.His269Arg
XR_001753134.1:n.1030A>G
XR_001753135.1:n.1030A>G
XR_001753136.1:n.1030A>G
NM_173844.3:c.806A>G	NP_776216.1:p.His269Arg