Canonical Allele Identifier: CA2396269138

Gene: RTN4R

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242640C= , CM000684.2:g.20242640C=	GRCh38
NC_000022.10:g.20230163C= , CM000684.1:g.20230163C=	GRCh37
NC_000022.9:g.18610163C=	NCBI36
NG_012176.1:g.30654G=
NG_012176.2:g.30654G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.493G= MANE Select	ENSP00000043402.7:p.Ala165=
ENST00000043402.7:c.493G=	ENSP00000043402.7:p.Ala165=
ENST00000416372.5:c.552G=
ENST00000425986.1:c.750G=
ENST00000469601.1:n.629G=
NM_023004.5:c.493G=	NP_075380.1:p.Ala165=
NM_023004.6:c.493G= MANE Select	NP_075380.1:p.Ala165=