Canonical Allele Identifier: CA2396269083
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242509T= , CM000684.2:g.20242509T= GRCh38
NC_000022.10:g.20230032T= , CM000684.1:g.20230032T= GRCh37
NC_000022.9:g.18610032T= NCBI36
NG_012176.1:g.30785A=
NG_012176.2:g.30785A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.624A= MANE Select ENSP00000043402.7:p.Leu208=
ENST00000043402.7:c.624A= ENSP00000043402.7:p.Leu208=
ENST00000416372.5:c.683A=
ENST00000425986.1:c.881A=
NM_023004.5:c.624A= NP_075380.1:p.Leu208=
NM_023004.6:c.624A= MANE Select NP_075380.1:p.Leu208=