Canonical Allele Identifier: CA2577329364
Gene: MAVS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857854T>G , CM000682.2:g.3857854T>G GRCh38
NC_000020.10:g.3838501T>G , CM000682.1:g.3838501T>G GRCh37
NC_000020.9:g.3786501T>G NCBI36
NG_030028.1:g.16056T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+45T>G MANE Select ENSP00000401980.2:n.292+45T>G
ENST00000416600.6:c.-132+3113T>G ENSP00000413749.2:n.-132+3113T>G
ENST00000428216.3:c.292+45T>G ENSP00000401980.2:n.292+45T>G
NM_001206491.1:c.-132+3113T>G NP_001193420.1:n.-132+3113T>G
NM_020746.4:c.292+45T>G NP_065797.2:n.292+45T>G
NR_037921.1:n.464+45T>G
NM_020746.5:c.292+45T>G MANE Select NP_065797.2:n.292+45T>G
NR_037921.2:n.429+45T>G
NM_001206491.2:c.-132+3113T>G NP_001193420.1:n.-132+3113T>G
NM_001385663.1:c.-256+45T>G NP_001372592.1:n.-256+45T>G