Canonical Allele Identifier: CA8977645

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58696477T>C , CM000680.2:g.58696477T>C	GRCh38
NC_000018.9:g.56363709T>C , CM000680.1:g.56363709T>C	GRCh37
NC_000018.8:g.54514689T>C	NCBI36
NG_033893.1:g.30092T>C
NG_033893.2:g.30092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697044.1:n.501T>C
ENST00000697098.1:n.231T>C
ENST00000697099.1:n.96T>C
ENST00000648670.1:c.278T>C	ENSP00000497173.1:p.Met93Thr
ENST00000649202.1:n.125T>C
ENST00000649217.2:c.488T>C MANE Select	ENSP00000497997.1:p.Met163Thr
ENST00000650045.1:c.488T>C	ENSP00000497036.1:p.Met163Thr
ENST00000345724.7:c.488T>C	ENSP00000304161.3:p.Met163Thr
ENST00000348428.7:c.488T>C	ENSP00000319279.4:p.Met163Thr
ENST00000591792.1:c.203T>C	ENSP00000467222.1:p.Met68Thr
NM_006785.3:c.488T>C	NP_006776.1:p.Met163Thr
NM_173844.2:c.488T>C	NP_776216.1:p.Met163Thr
XM_011525794.1:c.488T>C	XP_011524096.1:p.Met163Thr
XR_935190.1:n.712T>C
XR_935536.1:n.859+700A>G
XR_935537.1:n.859+700A>G
XR_935538.1:n.168+700A>G
NM_006785.4:c.488T>C MANE Select	NP_006776.1:p.Met163Thr
XR_001753134.1:n.712T>C
XR_001753135.1:n.712T>C
XR_001753136.1:n.712T>C
XR_935536.3:n.929+700A>G
XR_935537.2:n.929+700A>G
NM_173844.3:c.488T>C	NP_776216.1:p.Met163Thr