Canonical Allele Identifier: CA2346769739

Gene: MAVS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857810G= , CM000682.2:g.3857810G=	GRCh38
NC_000020.10:g.3838457G= , CM000682.1:g.3838457G=	GRCh37
NC_000020.9:g.3786457G=	NCBI36
NG_030028.1:g.16012G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.292+1G= MANE Select	ENSP00000401980.2:n.292+1G=
ENST00000416600.6:c.-132+3069G=	ENSP00000413749.2:n.-132+3069G=
ENST00000428216.3:c.292+1G=	ENSP00000401980.2:n.292+1G=
NM_001206491.1:c.-132+3069G=	NP_001193420.1:n.-132+3069G=
NM_020746.4:c.292+1G=	NP_065797.2:n.292+1G=
NR_037921.1:n.464+1G=
NM_020746.5:c.292+1G= MANE Select	NP_065797.2:n.292+1G=
NR_037921.2:n.429+1G=
NM_001206491.2:c.-132+3069G=	NP_001193420.1:n.-132+3069G=
NM_001385663.1:c.-256+1G=	NP_001372592.1:n.-256+1G=