Canonical Allele Identifier: CA2838334614
Gene: MAVS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3865650C>A , CM000682.2:g.3865650C>A GRCh38
NC_000020.10:g.3846297C>A , CM000682.1:g.3846297C>A GRCh37
NC_000020.9:g.3794297C>A NCBI36
NG_030028.1:g.23852C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.1159-33C>A MANE Select ENSP00000401980.2:n.1159-33C>A
ENST00000416600.6:c.736-33C>A ENSP00000413749.2:n.736-33C>A
ENST00000428216.3:c.1159-33C>A ENSP00000401980.2:n.1159-33C>A
NM_001206491.1:c.736-33C>A NP_001193420.1:n.736-33C>A
NM_020746.4:c.1159-33C>A NP_065797.2:n.1159-33C>A
NR_037921.1:n.1158-33C>A
NM_020746.5:c.1159-33C>A MANE Select NP_065797.2:n.1159-33C>A
NR_037921.2:n.1123-33C>A
NM_001206491.2:c.736-33C>A NP_001193420.1:n.736-33C>A
NM_001385663.1:c.736-33C>A NP_001372592.1:n.736-33C>A