Canonical Allele Identifier: CA9750022

Gene: MAVS

Linked Data

• dbSNP Id: rs764361176
• ExAC: 20:3838468 G / A
• MyVariant Identifiers: chr20:g.3838468G>A (hg19) ; chr20:g.3857821G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857821G>A , CM000682.2:g.3857821G>A	GRCh38
NC_000020.10:g.3838468G>A , CM000682.1:g.3838468G>A	GRCh37
NC_000020.9:g.3786468G>A	NCBI36
NG_030028.1:g.16023G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.292+12G>A MANE Select	ENSP00000401980.2:n.292+12G>A
ENST00000416600.6:c.-132+3080G>A	ENSP00000413749.2:n.-132+3080G>A
ENST00000428216.3:c.292+12G>A	ENSP00000401980.2:n.292+12G>A
NM_001206491.1:c.-132+3080G>A	NP_001193420.1:n.-132+3080G>A
NM_020746.4:c.292+12G>A	NP_065797.2:n.292+12G>A
NR_037921.1:n.464+12G>A
NM_020746.5:c.292+12G>A MANE Select	NP_065797.2:n.292+12G>A
NR_037921.2:n.429+12G>A
NM_001206491.2:c.-132+3080G>A	NP_001193420.1:n.-132+3080G>A
NM_001385663.1:c.-256+12G>A	NP_001372592.1:n.-256+12G>A