Canonical Allele Identifier: CA2346769727

Gene: MAVS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857783C= , CM000682.2:g.3857783C=	GRCh38
NC_000020.10:g.3838430C= , CM000682.1:g.3838430C=	GRCh37
NC_000020.9:g.3786430C=	NCBI36
NG_030028.1:g.15985C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.266C= MANE Select	ENSP00000401980.2:p.Ala89=
ENST00000416600.6:c.-132+3042C=	ENSP00000413749.2:n.-132+3042C=
ENST00000428216.3:c.266C=	ENSP00000401980.2:p.Ala89=
NM_001206491.1:c.-132+3042C=	NP_001193420.1:n.-132+3042C=
NM_020746.4:c.266C=	NP_065797.2:p.Ala89=
NR_037921.1:n.438C=
NM_020746.5:c.266C= MANE Select	NP_065797.2:p.Ala89=
NR_037921.2:n.403C=
NM_001206491.2:c.-132+3042C=	NP_001193420.1:n.-132+3042C=
NM_001385663.1:c.-282C=	NP_001372592.1:n.-282C=