Canonical Allele Identifier: CA8977697

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58709392G>A , CM000680.2:g.58709392G>A	GRCh38
NC_000018.9:g.56376624G>A , CM000680.1:g.56376624G>A	GRCh37
NC_000018.8:g.54527604G>A	NCBI36
NG_033893.1:g.43007G>A
NG_033893.2:g.43007G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697045.1:n.56G>A
ENST00000697098.1:n.407G>A
ENST00000697099.1:n.272G>A
ENST00000648670.1:c.440-584G>A	ENSP00000497173.1:n.440-584G>A
ENST00000649125.1:n.71G>A
ENST00000649202.1:n.301G>A
ENST00000649217.2:c.664G>A MANE Select	ENSP00000497997.1:p.Val222Ile
ENST00000650045.1:c.664G>A	ENSP00000497036.1:p.Val222Ile
ENST00000345724.7:c.664G>A	ENSP00000304161.3:p.Val222Ile
ENST00000348428.7:c.664G>A	ENSP00000319279.4:p.Val222Ile
NM_006785.3:c.664G>A	NP_006776.1:p.Val222Ile
NM_173844.2:c.664G>A	NP_776216.1:p.Val222Ile
XM_011525794.1:c.664G>A	XP_011524096.1:p.Val222Ile
XR_935190.1:n.888G>A
XR_935538.1:n.78-12125C>T
NM_006785.4:c.664G>A MANE Select	NP_006776.1:p.Val222Ile
XR_001753134.1:n.888G>A
XR_001753135.1:n.888G>A
XR_001753136.1:n.888G>A
NM_173844.3:c.664G>A	NP_776216.1:p.Val222Ile