Canonical Allele Identifier: CA311065090

Gene: MAVS

Linked Data

• dbSNP Id: rs33974977
• MyVariant Identifiers: chr20:g.3838206_3838207insT (hg19) ; chr20:g.3857559_3857560insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857559_3857560insT , CM000682.2:g.3857559_3857560insT	GRCh38
NC_000020.10:g.3838206_3838207insT , CM000682.1:g.3838206_3838207insT	GRCh37
NC_000020.9:g.3786206_3786207insT	NCBI36
NG_030028.1:g.15761_15762insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.118-76_118-75insT MANE Select	ENSP00000401980.2:n.118-76_118-75insT
ENST00000416600.6:c.-132+2818_-132+2819insT	ENSP00000413749.2:n.-132+2818_-132+2819insT
ENST00000428216.3:c.118-76_118-75insT	ENSP00000401980.2:n.118-76_118-75insT
NM_001206491.1:c.-132+2818_-132+2819insT	NP_001193420.1:n.-132+2818_-132+2819insT
NM_020746.4:c.118-76_118-75insT	NP_065797.2:n.118-76_118-75insT
NR_037921.1:n.290-76_290-75insT
NM_020746.5:c.118-76_118-75insT MANE Select	NP_065797.2:n.118-76_118-75insT
NR_037921.2:n.255-76_255-75insT
NM_001206491.2:c.-132+2818_-132+2819insT	NP_001193420.1:n.-132+2818_-132+2819insT
NM_001385663.1:c.-430-76_-430-75insT	NP_001372592.1:n.-430-76_-430-75insT