Canonical Allele Identifier: CA2818411381
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242393dup , CM000684.2:g.20242393dup GRCh38
NC_000022.10:g.20229916dup , CM000684.1:g.20229916dup GRCh37
NC_000022.9:g.18609916dup NCBI36
NG_012176.1:g.30906dup
NG_012176.2:g.30906dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.745dup MANE Select ENSP00000043402.7:p.Leu249ProfsTer17
ENST00000043402.7:c.745dup ENSP00000043402.7:p.Leu249ProfsTer17
ENST00000416372.5:c.804dup
ENST00000425986.1:c.1002dup
NM_023004.5:c.745dup NP_075380.1:p.Leu249ProfsTer17
NM_023004.6:c.745dup MANE Select NP_075380.1:p.Leu249ProfsTer17