Canonical Allele Identifier: CA8977659

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58700444C>A , CM000680.2:g.58700444C>A	GRCh38
NC_000018.9:g.56367676C>A , CM000680.1:g.56367676C>A	GRCh37
NC_000018.8:g.54518656C>A	NCBI36
NG_033893.1:g.34059C>A
NG_033893.2:g.34059C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697044.1:n.515C>A
ENST00000697098.1:n.245C>A
ENST00000697099.1:n.110C>A
ENST00000648670.1:c.292C>A	ENSP00000497173.1:p.Pro98Thr
ENST00000649202.1:n.139C>A
ENST00000649217.2:c.502C>A MANE Select	ENSP00000497997.1:p.Pro168Thr
ENST00000650045.1:c.502C>A	ENSP00000497036.1:p.Pro168Thr
ENST00000345724.7:c.502C>A	ENSP00000304161.3:p.Pro168Thr
ENST00000348428.7:c.502C>A	ENSP00000319279.4:p.Pro168Thr
ENST00000591792.1:c.217C>A	ENSP00000467222.1:p.Pro73Thr
NM_006785.3:c.502C>A	NP_006776.1:p.Pro168Thr
NM_173844.2:c.502C>A	NP_776216.1:p.Pro168Thr
XM_011525794.1:c.502C>A	XP_011524096.1:p.Pro168Thr
XR_935190.1:n.726C>A
XR_935538.1:n.78-3177G>T
NM_006785.4:c.502C>A MANE Select	NP_006776.1:p.Pro168Thr
XR_001753134.1:n.726C>A
XR_001753135.1:n.726C>A
XR_001753136.1:n.726C>A
NM_173844.3:c.502C>A	NP_776216.1:p.Pro168Thr