Canonical Allele Identifier: CA321807096
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs373097337
MyVariant Identifiers: chr21:g.45876668_45876669insGG (hg19) chr21:g.44456785_44456786insGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456786_44456787insGG , CM000683.2:g.44456786_44456787insGG GRCh38
NC_000021.8:g.45876669_45876670insGG , CM000683.1:g.45876669_45876670insGG GRCh37
NC_000021.7:g.44701097_44701098insGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.142_143insGG MANE Select ENSP00000291592.4:p.Val48GlyfsTer23
ENST00000291592.5:c.142_143insGG ENSP00000291592.4:p.Val48GlyfsTer23
NM_030891.4:c.142_143insGG NP_112153.1:p.Val48GlyfsTer23
NM_030891.5:c.142_143insGG NP_112153.1:p.Val48GlyfsTer23
NM_030891.6:c.142_143insGG MANE Select NP_112153.1:p.Val48GlyfsTer23
Search 100 bp 5'
Search 100 bp 3'