Canonical Allele Identifier: CA2346769786
Gene: MAVS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857878T= , CM000682.2:g.3857878T= GRCh38
NC_000020.10:g.3838525T= , CM000682.1:g.3838525T= GRCh37
NC_000020.9:g.3786525T= NCBI36
NG_030028.1:g.16080T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+69T= MANE Select ENSP00000401980.2:n.292+69T=
ENST00000416600.6:c.-132+3137T= ENSP00000413749.2:n.-132+3137T=
ENST00000428216.3:c.292+69T= ENSP00000401980.2:n.292+69T=
NM_001206491.1:c.-132+3137T= NP_001193420.1:n.-132+3137T=
NM_020746.4:c.292+69T= NP_065797.2:n.292+69T=
NR_037921.1:n.464+69T=
NM_020746.5:c.292+69T= MANE Select NP_065797.2:n.292+69T=
NR_037921.2:n.429+69T=
NM_001206491.2:c.-132+3137T= NP_001193420.1:n.-132+3137T=
NM_001385663.1:c.-256+69T= NP_001372592.1:n.-256+69T=
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