Canonical Allele Identifier: CA2651759254

Gene: MAVS

Linked Data

• gnomAD v4: 20-3857815-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857815_3857816insAG , CM000682.2:g.3857815_3857816insAG	GRCh38
NC_000020.10:g.3838462_3838463insAG , CM000682.1:g.3838462_3838463insAG	GRCh37
NC_000020.9:g.3786462_3786463insAG	NCBI36
NG_030028.1:g.16017_16018insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.292+6_292+7insAG MANE Select	ENSP00000401980.2:n.292+6_292+7insAG
ENST00000416600.6:c.-132+3074_-132+3075insAG	ENSP00000413749.2:n.-132+3074_-132+3075insAG
ENST00000428216.3:c.292+6_292+7insAG	ENSP00000401980.2:n.292+6_292+7insAG
NM_001206491.1:c.-132+3074_-132+3075insAG	NP_001193420.1:n.-132+3074_-132+3075insAG
NM_020746.4:c.292+6_292+7insAG	NP_065797.2:n.292+6_292+7insAG
NR_037921.1:n.464+6_464+7insAG
NM_020746.5:c.292+6_292+7insAG MANE Select	NP_065797.2:n.292+6_292+7insAG
NR_037921.2:n.429+6_429+7insAG
NM_001206491.2:c.-132+3074_-132+3075insAG	NP_001193420.1:n.-132+3074_-132+3075insAG
NM_001385663.1:c.-256+6_-256+7insAG	NP_001372592.1:n.-256+6_-256+7insAG