Canonical Allele Identifier: CA410712876
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242670C>T , CM000684.2:g.20242670C>T GRCh38
NC_000022.10:g.20230193C>T , CM000684.1:g.20230193C>T GRCh37
NC_000022.9:g.18610193C>T NCBI36
NG_012176.1:g.30624G>A
NG_012176.2:g.30624G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.463G>A MANE Select ENSP00000043402.7:p.Ala155Thr
ENST00000043402.7:c.463G>A ENSP00000043402.7:p.Ala155Thr
ENST00000416372.5:c.522G>A
ENST00000425986.1:c.720G>A
ENST00000469601.1:n.599G>A
NM_023004.5:c.463G>A NP_075380.1:p.Ala155Thr
NM_023004.6:c.463G>A MANE Select NP_075380.1:p.Ala155Thr