Canonical Allele Identifier: CA2396269105
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242559T= , CM000684.2:g.20242559T= GRCh38
NC_000022.10:g.20230082T= , CM000684.1:g.20230082T= GRCh37
NC_000022.9:g.18610082T= NCBI36
NG_012176.1:g.30735A=
NG_012176.2:g.30735A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.574A= MANE Select ENSP00000043402.7:p.Ser192=
ENST00000043402.7:c.574A= ENSP00000043402.7:p.Ser192=
ENST00000416372.5:c.633A=
ENST00000425986.1:c.831A=
NM_023004.5:c.574A= NP_075380.1:p.Ser192=
NM_023004.6:c.574A= MANE Select NP_075380.1:p.Ser192=