Canonical Allele Identifier: CA2396269032

Gene: RTN4R

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242388G= , CM000684.2:g.20242388G=	GRCh38
NC_000022.10:g.20229911G= , CM000684.1:g.20229911G=	GRCh37
NC_000022.9:g.18609911G=	NCBI36
NG_012176.1:g.30906C=
NG_012176.2:g.30906C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.745C= MANE Select	ENSP00000043402.7:p.Leu249=
ENST00000043402.7:c.745C=	ENSP00000043402.7:p.Leu249=
ENST00000416372.5:c.804C=
ENST00000425986.1:c.1002C=
NM_023004.5:c.745C=	NP_075380.1:p.Leu249=
NM_023004.6:c.745C= MANE Select	NP_075380.1:p.Leu249=