Canonical Allele Identifier: CA2346769664
Gene: MAVS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857658A= , CM000682.2:g.3857658A= GRCh38
NC_000020.10:g.3838305A= , CM000682.1:g.3838305A= GRCh37
NC_000020.9:g.3786305A= NCBI36
NG_030028.1:g.15860A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.141A= MANE Select ENSP00000401980.2:p.Thr47=
ENST00000416600.6:c.-132+2917A= ENSP00000413749.2:n.-132+2917A=
ENST00000428216.3:c.141A= ENSP00000401980.2:p.Thr47=
NM_001206491.1:c.-132+2917A= NP_001193420.1:n.-132+2917A=
NM_020746.4:c.141A= NP_065797.2:p.Thr47=
NR_037921.1:n.313A=
NM_020746.5:c.141A= MANE Select NP_065797.2:p.Thr47=
NR_037921.2:n.278A=
NM_001206491.2:c.-132+2917A= NP_001193420.1:n.-132+2917A=
NM_001385663.1:c.-407A= NP_001372592.1:n.-407A=