Canonical Allele Identifier: CA2396269206
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242803C= , CM000684.2:g.20242803C= GRCh38
NC_000022.10:g.20230326C= , CM000684.1:g.20230326C= GRCh37
NC_000022.9:g.18610326C= NCBI36
NG_012176.1:g.30491G=
NG_012176.2:g.30491G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.330G= MANE Select ENSP00000043402.7:p.Leu110=
ENST00000043402.7:c.330G= ENSP00000043402.7:p.Leu110=
ENST00000416372.5:c.389G=
ENST00000425986.1:c.587G=
ENST00000469601.1:n.466G=
NM_023004.5:c.330G= NP_075380.1:p.Leu110=
NM_023004.6:c.330G= MANE Select NP_075380.1:p.Leu110=