Canonical Allele Identifier: CA2396269200
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242779G= , CM000684.2:g.20242779G= GRCh38
NC_000022.10:g.20230302G= , CM000684.1:g.20230302G= GRCh37
NC_000022.9:g.18610302G= NCBI36
NG_012176.1:g.30515C=
NG_012176.2:g.30515C=

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.354C= MANE Select ENSP00000043402.7:p.Leu118=
ENST00000043402.7:c.354C= ENSP00000043402.7:p.Leu118=
ENST00000416372.5:c.413C=
ENST00000425986.1:c.611C=
ENST00000469601.1:n.490C=
NM_023004.5:c.354C= NP_075380.1:p.Leu118=
NM_023004.6:c.354C= MANE Select NP_075380.1:p.Leu118=