Canonical Allele Identifier: CA2346769732

Gene: MAVS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857800T= , CM000682.2:g.3857800T=	GRCh38
NC_000020.10:g.3838447T= , CM000682.1:g.3838447T=	GRCh37
NC_000020.9:g.3786447T=	NCBI36
NG_030028.1:g.16002T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.283T= MANE Select	ENSP00000401980.2:p.Tyr95=
ENST00000416600.6:c.-132+3059T=	ENSP00000413749.2:n.-132+3059T=
ENST00000428216.3:c.283T=	ENSP00000401980.2:p.Tyr95=
NM_001206491.1:c.-132+3059T=	NP_001193420.1:n.-132+3059T=
NM_020746.4:c.283T=	NP_065797.2:p.Tyr95=
NR_037921.1:n.455T=
NM_020746.5:c.283T= MANE Select	NP_065797.2:p.Tyr95=
NR_037921.2:n.420T=
NM_001206491.2:c.-132+3059T=	NP_001193420.1:n.-132+3059T=
NM_001385663.1:c.-265T=	NP_001372592.1:n.-265T=