Canonical Allele Identifier: CA410712709
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242622C>T , CM000684.2:g.20242622C>T GRCh38
NC_000022.10:g.20230145C>T , CM000684.1:g.20230145C>T GRCh37
NC_000022.9:g.18610145C>T NCBI36
NG_012176.1:g.30672G>A
NG_012176.2:g.30672G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.511G>A MANE Select ENSP00000043402.7:p.Asp171Asn
ENST00000043402.7:c.511G>A ENSP00000043402.7:p.Asp171Asn
ENST00000416372.5:c.570G>A
ENST00000425986.1:c.768G>A
ENST00000469601.1:n.647G>A
NM_023004.5:c.511G>A NP_075380.1:p.Asp171Asn
NM_023004.6:c.511G>A MANE Select NP_075380.1:p.Asp171Asn