Canonical Allele Identifier: CA1396954452
Gene: LRRC58 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120325040C= , CM000665.2:g.120325040C= GRCh38
NC_000003.11:g.120043887C= , CM000665.1:g.120043887C= GRCh37
NC_000003.10:g.121526577C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295628.4:c.*6160G= MANE Select ENSP00000295628.3:n.*6160G=
ENST00000295628.3:c.*6160G= ENSP00000295628.3:n.*6160G=
NM_001099678.1:c.*6160G= NP_001093148.1:n.*6160G=
NM_001099678.2:c.*6160G= MANE Select NP_001093148.1:n.*6160G=
Search 100 bp 5'
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