Canonical Allele Identifier: CA3861426
Gene: LRRC1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53922787T>G , CM000668.2:g.53922787T>G GRCh38
NC_000006.11:g.53787585T>G , CM000668.1:g.53787585T>G GRCh37
NC_000006.10:g.53895544T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370888.6:c.1569T>G MANE Select ENSP00000359925.1:p.Ser523=
ENST00000370888.5:c.1569T>G ENSP00000359925.1:p.Ser523=
NM_018214.4:c.1569T>G NP_060684.4:p.Ser523=
XM_011514726.1:c.1569T>G XP_011513028.1:p.Ser523=
XM_011514727.1:c.1392T>G XP_011513029.1:p.Ser464=
XM_011514726.2:c.1569T>G XP_011513028.1:p.Ser523=
XM_011514727.2:c.1392T>G XP_011513029.1:p.Ser464=
XR_001743504.1:n.2207T>G
NM_018214.5:c.1569T>G MANE Select NP_060684.4:p.Ser523=