Canonical Allele Identifier: CA2396269029

Gene: RTN4R

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242384C= , CM000684.2:g.20242384C=	GRCh38
NC_000022.10:g.20229907C= , CM000684.1:g.20229907C=	GRCh37
NC_000022.9:g.18609907C=	NCBI36
NG_012176.1:g.30910G=
NG_012176.2:g.30910G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.749G= MANE Select	ENSP00000043402.7:p.Arg250=
ENST00000043402.7:c.749G=	ENSP00000043402.7:p.Arg250=
ENST00000416372.5:c.808G=
ENST00000425986.1:c.1006G=
NM_023004.5:c.749G=	NP_075380.1:p.Arg250=
NM_023004.6:c.749G= MANE Select	NP_075380.1:p.Arg250=