Canonical Allele Identifier: CA2577329362
Gene: MAVS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857850del , CM000682.2:g.3857850del GRCh38
NC_000020.10:g.3838497del , CM000682.1:g.3838497del GRCh37
NC_000020.9:g.3786497del NCBI36
NG_030028.1:g.16052del

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+41del MANE Select ENSP00000401980.2:n.292+41del
ENST00000416600.6:c.-132+3109del ENSP00000413749.2:n.-132+3109del
ENST00000428216.3:c.292+41del ENSP00000401980.2:n.292+41del
NM_001206491.1:c.-132+3109del NP_001193420.1:n.-132+3109del
NM_020746.4:c.292+41del NP_065797.2:n.292+41del
NR_037921.1:n.464+41del
NM_020746.5:c.292+41del MANE Select NP_065797.2:n.292+41del
NR_037921.2:n.429+41del
NM_001206491.2:c.-132+3109del NP_001193420.1:n.-132+3109del
NM_001385663.1:c.-256+41del NP_001372592.1:n.-256+41del