Canonical Allele Identifier: CA410712780
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242644G>C , CM000684.2:g.20242644G>C GRCh38
NC_000022.10:g.20230167G>C , CM000684.1:g.20230167G>C GRCh37
NC_000022.9:g.18610167G>C NCBI36
NG_012176.1:g.30650C>G
NG_012176.2:g.30650C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.489C>G MANE Select ENSP00000043402.7:p.Asp163Glu
ENST00000043402.7:c.489C>G ENSP00000043402.7:p.Asp163Glu
ENST00000416372.5:c.548C>G
ENST00000425986.1:c.746C>G
ENST00000469601.1:n.625C>G
NM_023004.5:c.489C>G NP_075380.1:p.Asp163Glu
NM_023004.6:c.489C>G MANE Select NP_075380.1:p.Asp163Glu