Canonical Allele Identifier: CA2346769783
Gene: MAVS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857876T= , CM000682.2:g.3857876T= GRCh38
NC_000020.10:g.3838523T= , CM000682.1:g.3838523T= GRCh37
NC_000020.9:g.3786523T= NCBI36
NG_030028.1:g.16078T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.292+67T= MANE Select ENSP00000401980.2:n.292+67T=
ENST00000416600.6:c.-132+3135T= ENSP00000413749.2:n.-132+3135T=
ENST00000428216.3:c.292+67T= ENSP00000401980.2:n.292+67T=
NM_001206491.1:c.-132+3135T= NP_001193420.1:n.-132+3135T=
NM_020746.4:c.292+67T= NP_065797.2:n.292+67T=
NR_037921.1:n.464+67T=
NM_020746.5:c.292+67T= MANE Select NP_065797.2:n.292+67T=
NR_037921.2:n.429+67T=
NM_001206491.2:c.-132+3135T= NP_001193420.1:n.-132+3135T=
NM_001385663.1:c.-256+67T= NP_001372592.1:n.-256+67T=
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