Canonical Allele Identifier: CA300937364

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58681224C>G , CM000680.2:g.58681224C>G	GRCh38
NC_000018.9:g.56348456C>G , CM000680.1:g.56348456C>G	GRCh37
NC_000018.8:g.54499436C>G	NCBI36
NG_033893.1:g.14839C>G
NG_033893.2:g.14839C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697044.1:n.277C>G
ENST00000697098.1:n.7C>G
ENST00000648670.1:c.54C>G	ENSP00000497173.1:p.Pro18=
ENST00000649217.2:c.264C>G MANE Select	ENSP00000497997.1:p.Pro88=
ENST00000650045.1:c.264C>G	ENSP00000497036.1:p.Pro88=
ENST00000345724.7:c.264C>G	ENSP00000304161.3:p.Pro88=
ENST00000348428.7:c.264C>G	ENSP00000319279.4:p.Pro88=
ENST00000591792.1:c.-22C>G	ENSP00000467222.1:n.-22C>G
NM_006785.3:c.264C>G	NP_006776.1:p.Pro88=
NM_173844.2:c.264C>G	NP_776216.1:p.Pro88=
XM_011525794.1:c.264C>G	XP_011524096.1:p.Pro88=
XR_935190.1:n.488C>G
XR_935536.1:n.860-648G>C
XR_935537.1:n.860-648G>C
XR_935538.1:n.169-648G>C
NM_006785.4:c.264C>G MANE Select	NP_006776.1:p.Pro88=
XR_001753134.1:n.488C>G
XR_001753135.1:n.488C>G
XR_001753136.1:n.488C>G
XR_935536.3:n.930-648G>C
XR_935537.2:n.930-648G>C
NM_173844.3:c.264C>G	NP_776216.1:p.Pro88=