Canonical Allele Identifier: CA2346769608

Gene: MAVS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857547A= , CM000682.2:g.3857547A=	GRCh38
NC_000020.10:g.3838194A= , CM000682.1:g.3838194A=	GRCh37
NC_000020.9:g.3786194A=	NCBI36
NG_030028.1:g.15749A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.118-88A= MANE Select	ENSP00000401980.2:n.118-88A=
ENST00000416600.6:c.-132+2806A=	ENSP00000413749.2:n.-132+2806A=
ENST00000428216.3:c.118-88A=	ENSP00000401980.2:n.118-88A=
NM_001206491.1:c.-132+2806A=	NP_001193420.1:n.-132+2806A=
NM_020746.4:c.118-88A=	NP_065797.2:n.118-88A=
NR_037921.1:n.290-88A=
NM_020746.5:c.118-88A= MANE Select	NP_065797.2:n.118-88A=
NR_037921.2:n.255-88A=
NM_001206491.2:c.-132+2806A=	NP_001193420.1:n.-132+2806A=
NM_001385663.1:c.-430-88A=	NP_001372592.1:n.-430-88A=