Canonical Allele Identifier: CA2396269126

Gene: RTN4R

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242609C= , CM000684.2:g.20242609C=	GRCh38
NC_000022.10:g.20230132C= , CM000684.1:g.20230132C=	GRCh37
NC_000022.9:g.18610132C=	NCBI36
NG_012176.1:g.30685G=
NG_012176.2:g.30685G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.524G= MANE Select	ENSP00000043402.7:p.Arg175=
ENST00000043402.7:c.524G=	ENSP00000043402.7:p.Arg175=
ENST00000416372.5:c.583G=
ENST00000425986.1:c.781G=
ENST00000469601.1:n.660G=
NM_023004.5:c.524G=	NP_075380.1:p.Arg175=
NM_023004.6:c.524G= MANE Select	NP_075380.1:p.Arg175=