Canonical Allele Identifier: CA408118513
Gene: MAVS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857663C>G , CM000682.2:g.3857663C>G GRCh38
NC_000020.10:g.3838310C>G , CM000682.1:g.3838310C>G GRCh37
NC_000020.9:g.3786310C>G NCBI36
NG_030028.1:g.15865C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.146C>G MANE Select ENSP00000401980.2:p.Ser49Ter
ENST00000416600.6:c.-132+2922C>G ENSP00000413749.2:n.-132+2922C>G
ENST00000428216.3:c.146C>G ENSP00000401980.2:p.Ser49Ter
NM_001206491.1:c.-132+2922C>G NP_001193420.1:n.-132+2922C>G
NM_020746.4:c.146C>G NP_065797.2:p.Ser49Ter
NR_037921.1:n.318C>G
NM_020746.5:c.146C>G MANE Select NP_065797.2:p.Ser49Ter
NR_037921.2:n.283C>G
NM_001206491.2:c.-132+2922C>G NP_001193420.1:n.-132+2922C>G
NM_001385663.1:c.-402C>G NP_001372592.1:n.-402C>G