Canonical Allele Identifier: CA2396269199
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242778G= , CM000684.2:g.20242778G= GRCh38
NC_000022.10:g.20230301G= , CM000684.1:g.20230301G= GRCh37
NC_000022.9:g.18610301G= NCBI36
NG_012176.1:g.30516C=
NG_012176.2:g.30516C=

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.355C= MANE Select ENSP00000043402.7:p.Arg119=
ENST00000043402.7:c.355C= ENSP00000043402.7:p.Arg119=
ENST00000416372.5:c.414C=
ENST00000425986.1:c.612C=
ENST00000469601.1:n.491C=
NM_023004.5:c.355C= NP_075380.1:p.Arg119=
NM_023004.6:c.355C= MANE Select NP_075380.1:p.Arg119=