Canonical Allele Identifier: CA2346769619
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs2089821823

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857556_3857557insG , CM000682.2:g.3857556_3857557insG GRCh38
NC_000020.10:g.3838203_3838204insG , CM000682.1:g.3838203_3838204insG GRCh37
NC_000020.9:g.3786203_3786204insG NCBI36
NG_030028.1:g.15758_15759insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.118-79_118-78insG MANE Select ENSP00000401980.2:n.118-79_118-78insG
ENST00000416600.6:c.-132+2815_-132+2816insG ENSP00000413749.2:n.-132+2815_-132+2816insG
ENST00000428216.3:c.118-79_118-78insG ENSP00000401980.2:n.118-79_118-78insG
NM_001206491.1:c.-132+2815_-132+2816insG NP_001193420.1:n.-132+2815_-132+2816insG
NM_020746.4:c.118-79_118-78insG NP_065797.2:n.118-79_118-78insG
NR_037921.1:n.290-79_290-78insG
NM_020746.5:c.118-79_118-78insG MANE Select NP_065797.2:n.118-79_118-78insG
NR_037921.2:n.255-79_255-78insG
NM_001206491.2:c.-132+2815_-132+2816insG NP_001193420.1:n.-132+2815_-132+2816insG
NM_001385663.1:c.-430-79_-430-78insG NP_001372592.1:n.-430-79_-430-78insG