Canonical Allele Identifier: CA408119088
Gene: MAVS HGNC NCBI

Linked Data

COSMIC: COSM3799532
MyVariant Identifiers: chr20:g.3838402G>A (hg19) chr20:g.3857755G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857755G>A , CM000682.2:g.3857755G>A GRCh38
NC_000020.10:g.3838402G>A , CM000682.1:g.3838402G>A GRCh37
NC_000020.9:g.3786402G>A NCBI36
NG_030028.1:g.15957G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.238G>A MANE Select ENSP00000401980.2:p.Glu80Lys
ENST00000416600.6:c.-132+3014G>A ENSP00000413749.2:n.-132+3014G>A
ENST00000428216.3:c.238G>A ENSP00000401980.2:p.Glu80Lys
NM_001206491.1:c.-132+3014G>A NP_001193420.1:n.-132+3014G>A
NM_020746.4:c.238G>A NP_065797.2:p.Glu80Lys
NR_037921.1:n.410G>A
NM_020746.5:c.238G>A MANE Select NP_065797.2:p.Glu80Lys
NR_037921.2:n.375G>A
NM_001206491.2:c.-132+3014G>A NP_001193420.1:n.-132+3014G>A
NM_001385663.1:c.-310G>A NP_001372592.1:n.-310G>A
Search 100 bp 5'
Search 100 bp 3'