Canonical Allele Identifier: CA402572727
Gene: MALT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58700454A>G , CM000680.2:g.58700454A>G GRCh38
NC_000018.9:g.56367686A>G , CM000680.1:g.56367686A>G GRCh37
NC_000018.8:g.54518666A>G NCBI36
NG_033893.1:g.34069A>G
NG_033893.2:g.34069A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697044.1:n.525A>G
ENST00000697098.1:n.255A>G
ENST00000697099.1:n.120A>G
ENST00000648670.1:c.302A>G ENSP00000497173.1:p.Asn101Ser
ENST00000649202.1:n.149A>G
ENST00000649217.2:c.512A>G MANE Select ENSP00000497997.1:p.Asn171Ser
ENST00000650045.1:c.512A>G ENSP00000497036.1:p.Asn171Ser
ENST00000345724.7:c.512A>G ENSP00000304161.3:p.Asn171Ser
ENST00000348428.7:c.512A>G ENSP00000319279.4:p.Asn171Ser
ENST00000591792.1:c.227A>G ENSP00000467222.1:p.Asn76Ser
NM_006785.3:c.512A>G NP_006776.1:p.Asn171Ser
NM_173844.2:c.512A>G NP_776216.1:p.Asn171Ser
XM_011525794.1:c.512A>G XP_011524096.1:p.Asn171Ser
XR_935190.1:n.736A>G
XR_935538.1:n.78-3187T>C
NM_006785.4:c.512A>G MANE Select NP_006776.1:p.Asn171Ser
XR_001753134.1:n.736A>G
XR_001753135.1:n.736A>G
XR_001753136.1:n.736A>G
NM_173844.3:c.512A>G NP_776216.1:p.Asn171Ser