Canonical Allele Identifier: CA2396269203
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242788A= , CM000684.2:g.20242788A= GRCh38
NC_000022.10:g.20230311A= , CM000684.1:g.20230311A= GRCh37
NC_000022.9:g.18610311A= NCBI36
NG_012176.1:g.30506T=
NG_012176.2:g.30506T=

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.345T= MANE Select ENSP00000043402.7:p.Asn115=
ENST00000043402.7:c.345T= ENSP00000043402.7:p.Asn115=
ENST00000416372.5:c.404T=
ENST00000425986.1:c.602T=
ENST00000469601.1:n.481T=
NM_023004.5:c.345T= NP_075380.1:p.Asn115=
NM_023004.6:c.345T= MANE Select NP_075380.1:p.Asn115=