Canonical Allele Identifier: CA10056001
Gene: LRRC3 HGNC NCBI

Linked Data

dbSNP Id: rs768017723
ExAC: 21:45876591 TTCC / T
gnomAD v2: 21-45876591-TTCC-T
gnomAD v3: 21-44456708-TTCC-T
gnomAD v4: 21-44456708-TTCC-T
MyVariant Identifiers: chr21:g.45876592_45876594del (hg19) chr21:g.44456709_44456711del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44456714_44456716del , CM000683.2:g.44456714_44456716del GRCh38
NC_000021.8:g.45876597_45876599del , CM000683.1:g.45876597_45876599del GRCh37
NC_000021.7:g.44701025_44701027del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291592.6:c.70_72del MANE Select ENSP00000291592.4:p.Leu24del
ENST00000291592.5:c.70_72del ENSP00000291592.4:p.Leu24del
NM_030891.4:c.70_72del NP_112153.1:p.Leu24del
NM_030891.5:c.70_72del NP_112153.1:p.Leu24del
NM_030891.6:c.70_72del MANE Select NP_112153.1:p.Leu24del
Search 100 bp 5'
Search 100 bp 3'