Canonical Allele Identifier: CA2346769768

Gene: MAVS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857851C= , CM000682.2:g.3857851C=	GRCh38
NC_000020.10:g.3838498C= , CM000682.1:g.3838498C=	GRCh37
NC_000020.9:g.3786498C=	NCBI36
NG_030028.1:g.16053C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.292+42C= MANE Select	ENSP00000401980.2:n.292+42C=
ENST00000416600.6:c.-132+3110C=	ENSP00000413749.2:n.-132+3110C=
ENST00000428216.3:c.292+42C=	ENSP00000401980.2:n.292+42C=
NM_001206491.1:c.-132+3110C=	NP_001193420.1:n.-132+3110C=
NM_020746.4:c.292+42C=	NP_065797.2:n.292+42C=
NR_037921.1:n.464+42C=
NM_020746.5:c.292+42C= MANE Select	NP_065797.2:n.292+42C=
NR_037921.2:n.429+42C=
NM_001206491.2:c.-132+3110C=	NP_001193420.1:n.-132+3110C=
NM_001385663.1:c.-256+42C=	NP_001372592.1:n.-256+42C=