Canonical Allele Identifier: CA2346769659

Gene: MAVS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857648C= , CM000682.2:g.3857648C=	GRCh38
NC_000020.10:g.3838295C= , CM000682.1:g.3838295C=	GRCh37
NC_000020.9:g.3786295C=	NCBI36
NG_030028.1:g.15850C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.131C= MANE Select	ENSP00000401980.2:p.Ala44=
ENST00000416600.6:c.-132+2907C=	ENSP00000413749.2:n.-132+2907C=
ENST00000428216.3:c.131C=	ENSP00000401980.2:p.Ala44=
NM_001206491.1:c.-132+2907C=	NP_001193420.1:n.-132+2907C=
NM_020746.4:c.131C=	NP_065797.2:p.Ala44=
NR_037921.1:n.303C=
NM_020746.5:c.131C= MANE Select	NP_065797.2:p.Ala44=
NR_037921.2:n.268C=
NM_001206491.2:c.-132+2907C=	NP_001193420.1:n.-132+2907C=
NM_001385663.1:c.-417C=	NP_001372592.1:n.-417C=