Canonical Allele Identifier: CA311065105
Gene: MAVS HGNC NCBI

Linked Data

dbSNP Id: rs111980275
MyVariant Identifiers: chr20:g.3838237del (hg19) chr20:g.3857590del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3857590del , CM000682.2:g.3857590del GRCh38
NC_000020.10:g.3838237del , CM000682.1:g.3838237del GRCh37
NC_000020.9:g.3786237del NCBI36
NG_030028.1:g.15792del

Transcript Alleles

HGVS Amino-acid Change
ENST00000428216.4:c.118-45del MANE Select ENSP00000401980.2:n.118-45del
ENST00000416600.6:c.-132+2849del ENSP00000413749.2:n.-132+2849del
ENST00000428216.3:c.118-45del ENSP00000401980.2:n.118-45del
NM_001206491.1:c.-132+2849del NP_001193420.1:n.-132+2849del
NM_020746.4:c.118-45del NP_065797.2:n.118-45del
NR_037921.1:n.290-45del
NM_020746.5:c.118-45del MANE Select NP_065797.2:n.118-45del
NR_037921.2:n.255-45del
NM_001206491.2:c.-132+2849del NP_001193420.1:n.-132+2849del
NM_001385663.1:c.-430-45del NP_001372592.1:n.-430-45del
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