Canonical Allele Identifier: CA1014898226

Gene: MAVS

Linked Data

• dbSNP Id: rs767040934
• gnomAD v3: 20-3857552-TC-T
• gnomAD v4: 20-3857552-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857558del , CM000682.2:g.3857558del	GRCh38
NC_000020.10:g.3838205del , CM000682.1:g.3838205del	GRCh37
NC_000020.9:g.3786205del	NCBI36
NG_030028.1:g.15760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.118-77del MANE Select	ENSP00000401980.2:n.118-77del
ENST00000416600.6:c.-132+2817del	ENSP00000413749.2:n.-132+2817del
ENST00000428216.3:c.118-77del	ENSP00000401980.2:n.118-77del
NM_001206491.1:c.-132+2817del	NP_001193420.1:n.-132+2817del
NM_020746.4:c.118-77del	NP_065797.2:n.118-77del
NR_037921.1:n.290-77del
NM_020746.5:c.118-77del MANE Select	NP_065797.2:n.118-77del
NR_037921.2:n.255-77del
NM_001206491.2:c.-132+2817del	NP_001193420.1:n.-132+2817del
NM_001385663.1:c.-430-77del	NP_001372592.1:n.-430-77del