Canonical Allele Identifier: CA2346769635
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs2089822301

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857594dup , CM000682.2:g.3857594dup GRCh38
NC_000020.10:g.3838241dup , CM000682.1:g.3838241dup GRCh37
NC_000020.9:g.3786241dup NCBI36
NG_030028.1:g.15796dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.118-41dup MANE Select ENSP00000401980.2:n.118-41dup
ENST00000416600.6:c.-132+2853dup ENSP00000413749.2:n.-132+2853dup
ENST00000428216.3:c.118-41dup ENSP00000401980.2:n.118-41dup
NM_001206491.1:c.-132+2853dup NP_001193420.1:n.-132+2853dup
NM_020746.4:c.118-41dup NP_065797.2:n.118-41dup
NR_037921.1:n.290-41dup
NM_020746.5:c.118-41dup MANE Select NP_065797.2:n.118-41dup
NR_037921.2:n.255-41dup
NM_001206491.2:c.-132+2853dup NP_001193420.1:n.-132+2853dup
NM_001385663.1:c.-430-41dup NP_001372592.1:n.-430-41dup