Canonical Allele Identifier: CA2396269129

Gene: RTN4R

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242616T= , CM000684.2:g.20242616T=	GRCh38
NC_000022.10:g.20230139T= , CM000684.1:g.20230139T=	GRCh37
NC_000022.9:g.18610139T=	NCBI36
NG_012176.1:g.30678A=
NG_012176.2:g.30678A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.517A= MANE Select	ENSP00000043402.7:p.Thr173=
ENST00000043402.7:c.517A=	ENSP00000043402.7:p.Thr173=
ENST00000416372.5:c.576A=
ENST00000425986.1:c.774A=
ENST00000469601.1:n.653A=
NM_023004.5:c.517A=	NP_075380.1:p.Thr173=
NM_023004.6:c.517A= MANE Select	NP_075380.1:p.Thr173=