Canonical Allele Identifier: CA8977613

Gene: MALT1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58681324C>T , CM000680.2:g.58681324C>T	GRCh38
NC_000018.9:g.56348556C>T , CM000680.1:g.56348556C>T	GRCh37
NC_000018.8:g.54499536C>T	NCBI36
NG_033893.1:g.14939C>T
NG_033893.2:g.14939C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697044.1:n.377C>T
ENST00000697098.1:n.107C>T
ENST00000648670.1:c.154C>T	ENSP00000497173.1:p.Leu52Phe
ENST00000649202.1:n.1C>T
ENST00000649217.2:c.364C>T MANE Select	ENSP00000497997.1:p.Leu122Phe
ENST00000650045.1:c.364C>T	ENSP00000497036.1:p.Leu122Phe
ENST00000345724.7:c.364C>T	ENSP00000304161.3:p.Leu122Phe
ENST00000348428.7:c.364C>T	ENSP00000319279.4:p.Leu122Phe
ENST00000591792.1:c.79C>T	ENSP00000467222.1:p.Leu27Phe
NM_006785.3:c.364C>T	NP_006776.1:p.Leu122Phe
NM_173844.2:c.364C>T	NP_776216.1:p.Leu122Phe
XM_011525794.1:c.364C>T	XP_011524096.1:p.Leu122Phe
XR_935190.1:n.588C>T
XR_935536.1:n.860-748G>A
XR_935537.1:n.860-748G>A
XR_935538.1:n.169-748G>A
NM_006785.4:c.364C>T MANE Select	NP_006776.1:p.Leu122Phe
XR_001753134.1:n.588C>T
XR_001753135.1:n.588C>T
XR_001753136.1:n.588C>T
XR_935536.3:n.930-748G>A
XR_935537.2:n.930-748G>A
NM_173844.3:c.364C>T	NP_776216.1:p.Leu122Phe