Canonical Allele Identifier: CA1011651
Community Standard Title: NM_014813.3(LRIG2):c.256C>T (p.Arg86Trp)
Gene: LRIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113091334C>T , CM000663.2:g.113091334C>T GRCh38
NC_000001.10:g.113633956C>T , CM000663.1:g.113633956C>T GRCh37
NC_000001.9:g.113435479C>T NCBI36
NG_042819.1:g.23165C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014813.3:c.256C>T MANE Select NP_055628.1:p.Arg86Trp
ENST00000361127.6:c.256C>T MANE Select ENSP00000355396.4:p.Arg86Trp
NM_001312686.1:c.-166C>T NP_001299615.1:n.-166C>T
NM_001312686.2:c.-166C>T NP_001299615.1:n.-166C>T
NM_014813.2:c.256C>T NP_055628.1:p.Arg86Trp
ENST00000361127.5:c.256C>T ENSP00000355396.4:p.Arg86Trp
XM_005271369.1:c.256C>T XP_005271426.1:p.Arg86Trp
XM_005271369.2:c.256C>T XP_005271426.1:p.Arg86Trp
XM_017002952.2:c.-1408C>T XP_016858441.1:n.-1408C>T
XM_024451227.1:c.-54C>T XP_024306995.1:n.-54C>T