Canonical Allele Identifier: CA1396954446
Gene: LRRC58 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120325018A= , CM000665.2:g.120325018A= GRCh38
NC_000003.11:g.120043865A= , CM000665.1:g.120043865A= GRCh37
NC_000003.10:g.121526555A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295628.4:c.*6182T= MANE Select ENSP00000295628.3:n.*6182T=
ENST00000295628.3:c.*6182T= ENSP00000295628.3:n.*6182T=
NM_001099678.1:c.*6182T= NP_001093148.1:n.*6182T=
NM_001099678.2:c.*6182T= MANE Select NP_001093148.1:n.*6182T=