Canonical Allele Identifier: CA780936129

Gene: MALT1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58716960T>A , CM000680.2:g.58716960T>A	GRCh38
NC_000018.9:g.56384192T>A , CM000680.1:g.56384192T>A	GRCh37
NC_000018.8:g.54535172T>A	NCBI36
NG_033893.1:g.50575T>A
NG_033893.2:g.50575T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697045.1:n.829+993T>A
ENST00000697046.1:n.127+993T>A
ENST00000697098.1:n.761+993T>A
ENST00000697099.1:n.626+993T>A
ENST00000648670.1:c.629+993T>A	ENSP00000497173.1:n.629+993T>A
ENST00000649125.1:n.844+993T>A
ENST00000649202.1:n.622+993T>A
ENST00000649217.2:c.1018+993T>A MANE Select	ENSP00000497997.1:n.1018+993T>A
ENST00000650045.1:c.1018+993T>A	ENSP00000497036.1:n.1018+993T>A
ENST00000345724.7:c.985+993T>A	ENSP00000304161.3:n.985+993T>A
ENST00000348428.7:c.1018+993T>A	ENSP00000319279.4:n.1018+993T>A
NM_006785.3:c.1018+993T>A	NP_006776.1:n.1018+993T>A
NM_173844.2:c.985+993T>A	NP_776216.1:n.985+993T>A
XM_011525794.1:c.1018+993T>A	XP_011524096.1:n.1018+993T>A
XR_935190.1:n.1242+993T>A
XR_935538.1:n.78-19693A>T
NM_006785.4:c.1018+993T>A MANE Select	NP_006776.1:n.1018+993T>A
XR_001753134.1:n.1242+993T>A
XR_001753135.1:n.1209+993T>A
XR_001753136.1:n.1242+993T>A
NM_173844.3:c.985+993T>A	NP_776216.1:n.985+993T>A