Canonical Allele Identifier: CA2346769719
Gene: MAVS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857771C= , CM000682.2:g.3857771C= GRCh38
NC_000020.10:g.3838418C= , CM000682.1:g.3838418C= GRCh37
NC_000020.9:g.3786418C= NCBI36
NG_030028.1:g.15973C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.254C= MANE Select ENSP00000401980.2:p.Ala85=
ENST00000416600.6:c.-132+3030C= ENSP00000413749.2:n.-132+3030C=
ENST00000428216.3:c.254C= ENSP00000401980.2:p.Ala85=
NM_001206491.1:c.-132+3030C= NP_001193420.1:n.-132+3030C=
NM_020746.4:c.254C= NP_065797.2:p.Ala85=
NR_037921.1:n.426C=
NM_020746.5:c.254C= MANE Select NP_065797.2:p.Ala85=
NR_037921.2:n.391C=
NM_001206491.2:c.-132+3030C= NP_001193420.1:n.-132+3030C=
NM_001385663.1:c.-294C= NP_001372592.1:n.-294C=