Canonical Allele Identifier: CA509425207

Gene: MAVS

Linked Data

• MyVariant Identifiers: chr20:g.3838299C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857652C>G , CM000682.2:g.3857652C>G	GRCh38
NC_000020.10:g.3838299C>G , CM000682.1:g.3838299C>G	GRCh37
NC_000020.9:g.3786299C>G	NCBI36
NG_030028.1:g.15854C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.135C>G MANE Select	ENSP00000401980.2:p.Thr45=
ENST00000416600.6:c.-132+2911C>G	ENSP00000413749.2:n.-132+2911C>G
ENST00000428216.3:c.135C>G	ENSP00000401980.2:p.Thr45=
NM_001206491.1:c.-132+2911C>G	NP_001193420.1:n.-132+2911C>G
NM_020746.4:c.135C>G	NP_065797.2:p.Thr45=
NR_037921.1:n.307C>G
NM_020746.5:c.135C>G MANE Select	NP_065797.2:p.Thr45=
NR_037921.2:n.272C>G
NM_001206491.2:c.-132+2911C>G	NP_001193420.1:n.-132+2911C>G
NM_001385663.1:c.-413C>G	NP_001372592.1:n.-413C>G