Canonical Allele Identifier: CA2651759220
Gene: MAVS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857582del , CM000682.2:g.3857582del GRCh38
NC_000020.10:g.3838229del , CM000682.1:g.3838229del GRCh37
NC_000020.9:g.3786229del NCBI36
NG_030028.1:g.15784del

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.118-53del MANE Select ENSP00000401980.2:n.118-53del
ENST00000416600.6:c.-132+2841del ENSP00000413749.2:n.-132+2841del
ENST00000428216.3:c.118-53del ENSP00000401980.2:n.118-53del
NM_001206491.1:c.-132+2841del NP_001193420.1:n.-132+2841del
NM_020746.4:c.118-53del NP_065797.2:n.118-53del
NR_037921.1:n.290-53del
NM_020746.5:c.118-53del MANE Select NP_065797.2:n.118-53del
NR_037921.2:n.255-53del
NM_001206491.2:c.-132+2841del NP_001193420.1:n.-132+2841del
NM_001385663.1:c.-430-53del NP_001372592.1:n.-430-53del