Canonical Allele Identifier: CA2346769723
Gene: MAVS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857776G= , CM000682.2:g.3857776G= GRCh38
NC_000020.10:g.3838423G= , CM000682.1:g.3838423G= GRCh37
NC_000020.9:g.3786423G= NCBI36
NG_030028.1:g.15978G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.259G= MANE Select ENSP00000401980.2:p.Glu87=
ENST00000416600.6:c.-132+3035G= ENSP00000413749.2:n.-132+3035G=
ENST00000428216.3:c.259G= ENSP00000401980.2:p.Glu87=
NM_001206491.1:c.-132+3035G= NP_001193420.1:n.-132+3035G=
NM_020746.4:c.259G= NP_065797.2:p.Glu87=
NR_037921.1:n.431G=
NM_020746.5:c.259G= MANE Select NP_065797.2:p.Glu87=
NR_037921.2:n.396G=
NM_001206491.2:c.-132+3035G= NP_001193420.1:n.-132+3035G=
NM_001385663.1:c.-289G= NP_001372592.1:n.-289G=