Canonical Allele Identifier: CA2346769616
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs930935126

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857555_3857556insT , CM000682.2:g.3857555_3857556insT GRCh38
NC_000020.10:g.3838202_3838203insT , CM000682.1:g.3838202_3838203insT GRCh37
NC_000020.9:g.3786202_3786203insT NCBI36
NG_030028.1:g.15757_15758insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.118-80_118-79insT MANE Select ENSP00000401980.2:n.118-80_118-79insT
ENST00000416600.6:c.-132+2814_-132+2815insT ENSP00000413749.2:n.-132+2814_-132+2815insT
ENST00000428216.3:c.118-80_118-79insT ENSP00000401980.2:n.118-80_118-79insT
NM_001206491.1:c.-132+2814_-132+2815insT NP_001193420.1:n.-132+2814_-132+2815insT
NM_020746.4:c.118-80_118-79insT NP_065797.2:n.118-80_118-79insT
NR_037921.1:n.290-80_290-79insT
NM_020746.5:c.118-80_118-79insT MANE Select NP_065797.2:n.118-80_118-79insT
NR_037921.2:n.255-80_255-79insT
NM_001206491.2:c.-132+2814_-132+2815insT NP_001193420.1:n.-132+2814_-132+2815insT
NM_001385663.1:c.-430-80_-430-79insT NP_001372592.1:n.-430-80_-430-79insT