Canonical Allele Identifier: CA509425382

Gene: MAVS

Linked Data

• MyVariant Identifiers: chr20:g.3838437C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857790C>T , CM000682.2:g.3857790C>T	GRCh38
NC_000020.10:g.3838437C>T , CM000682.1:g.3838437C>T	GRCh37
NC_000020.9:g.3786437C>T	NCBI36
NG_030028.1:g.15992C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.273C>T MANE Select	ENSP00000401980.2:p.Val91=
ENST00000416600.6:c.-132+3049C>T	ENSP00000413749.2:n.-132+3049C>T
ENST00000428216.3:c.273C>T	ENSP00000401980.2:p.Val91=
NM_001206491.1:c.-132+3049C>T	NP_001193420.1:n.-132+3049C>T
NM_020746.4:c.273C>T	NP_065797.2:p.Val91=
NR_037921.1:n.445C>T
NM_020746.5:c.273C>T MANE Select	NP_065797.2:p.Val91=
NR_037921.2:n.410C>T
NM_001206491.2:c.-132+3049C>T	NP_001193420.1:n.-132+3049C>T
NM_001385663.1:c.-275C>T	NP_001372592.1:n.-275C>T