Canonical Allele Identifier: CA2396269055
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242434C= , CM000684.2:g.20242434C= GRCh38
NC_000022.10:g.20229957C= , CM000684.1:g.20229957C= GRCh37
NC_000022.9:g.18609957C= NCBI36
NG_012176.1:g.30860G=
NG_012176.2:g.30860G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.699G= MANE Select ENSP00000043402.7:p.Leu233=
ENST00000043402.7:c.699G= ENSP00000043402.7:p.Leu233=
ENST00000416372.5:c.758G=
ENST00000425986.1:c.956G=
NM_023004.5:c.699G= NP_075380.1:p.Leu233=
NM_023004.6:c.699G= MANE Select NP_075380.1:p.Leu233=