Canonical Allele Identifier: CA2651759279
Gene: MAVS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857890del , CM000682.2:g.3857890del GRCh38
NC_000020.10:g.3838537del , CM000682.1:g.3838537del GRCh37
NC_000020.9:g.3786537del NCBI36
NG_030028.1:g.16092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+81del MANE Select ENSP00000401980.2:n.292+81del
ENST00000416600.6:c.-132+3149del ENSP00000413749.2:n.-132+3149del
ENST00000428216.3:c.292+81del ENSP00000401980.2:n.292+81del
NM_001206491.1:c.-132+3149del NP_001193420.1:n.-132+3149del
NM_020746.4:c.292+81del NP_065797.2:n.292+81del
NR_037921.1:n.464+81del
NM_020746.5:c.292+81del MANE Select NP_065797.2:n.292+81del
NR_037921.2:n.429+81del
NM_001206491.2:c.-132+3149del NP_001193420.1:n.-132+3149del
NM_001385663.1:c.-256+81del NP_001372592.1:n.-256+81del