Canonical Allele Identifier: CA509425363

Gene: MAVS

Linked Data

• MyVariant Identifiers: chr20:g.3838431C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857784C>A , CM000682.2:g.3857784C>A	GRCh38
NC_000020.10:g.3838431C>A , CM000682.1:g.3838431C>A	GRCh37
NC_000020.9:g.3786431C>A	NCBI36
NG_030028.1:g.15986C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.267C>A MANE Select	ENSP00000401980.2:p.Ala89=
ENST00000416600.6:c.-132+3043C>A	ENSP00000413749.2:n.-132+3043C>A
ENST00000428216.3:c.267C>A	ENSP00000401980.2:p.Ala89=
NM_001206491.1:c.-132+3043C>A	NP_001193420.1:n.-132+3043C>A
NM_020746.4:c.267C>A	NP_065797.2:p.Ala89=
NR_037921.1:n.439C>A
NM_020746.5:c.267C>A MANE Select	NP_065797.2:p.Ala89=
NR_037921.2:n.404C>A
NM_001206491.2:c.-132+3043C>A	NP_001193420.1:n.-132+3043C>A
NM_001385663.1:c.-281C>A	NP_001372592.1:n.-281C>A