Canonical Allele Identifier: CA402573097

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58709393T>C , CM000680.2:g.58709393T>C	GRCh38
NC_000018.9:g.56376625T>C , CM000680.1:g.56376625T>C	GRCh37
NC_000018.8:g.54527605T>C	NCBI36
NG_033893.1:g.43008T>C
NG_033893.2:g.43008T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697045.1:n.57T>C
ENST00000697098.1:n.408T>C
ENST00000697099.1:n.273T>C
ENST00000648670.1:c.440-583T>C	ENSP00000497173.1:n.440-583T>C
ENST00000649125.1:n.72T>C
ENST00000649202.1:n.302T>C
ENST00000649217.2:c.665T>C MANE Select	ENSP00000497997.1:p.Val222Ala
ENST00000650045.1:c.665T>C	ENSP00000497036.1:p.Val222Ala
ENST00000345724.7:c.665T>C	ENSP00000304161.3:p.Val222Ala
ENST00000348428.7:c.665T>C	ENSP00000319279.4:p.Val222Ala
NM_006785.3:c.665T>C	NP_006776.1:p.Val222Ala
NM_173844.2:c.665T>C	NP_776216.1:p.Val222Ala
XM_011525794.1:c.665T>C	XP_011524096.1:p.Val222Ala
XR_935190.1:n.889T>C
XR_935538.1:n.78-12126A>G
NM_006785.4:c.665T>C MANE Select	NP_006776.1:p.Val222Ala
XR_001753134.1:n.889T>C
XR_001753135.1:n.889T>C
XR_001753136.1:n.889T>C
NM_173844.3:c.665T>C	NP_776216.1:p.Val222Ala