Canonical Allele Identifier: CA408119155

Gene: MAVS

Linked Data

• MyVariant Identifiers: chr20:g.3838435G>A (hg19) ; chr20:g.3857788G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857788G>A , CM000682.2:g.3857788G>A	GRCh38
NC_000020.10:g.3838435G>A , CM000682.1:g.3838435G>A	GRCh37
NC_000020.9:g.3786435G>A	NCBI36
NG_030028.1:g.15990G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.271G>A MANE Select	ENSP00000401980.2:p.Val91Ile
ENST00000416600.6:c.-132+3047G>A	ENSP00000413749.2:n.-132+3047G>A
ENST00000428216.3:c.271G>A	ENSP00000401980.2:p.Val91Ile
NM_001206491.1:c.-132+3047G>A	NP_001193420.1:n.-132+3047G>A
NM_020746.4:c.271G>A	NP_065797.2:p.Val91Ile
NR_037921.1:n.443G>A
NM_020746.5:c.271G>A MANE Select	NP_065797.2:p.Val91Ile
NR_037921.2:n.408G>A
NM_001206491.2:c.-132+3047G>A	NP_001193420.1:n.-132+3047G>A
NM_001385663.1:c.-277G>A	NP_001372592.1:n.-277G>A