Canonical Allele Identifier: CA2396269124

Gene: RTN4R

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242606T= , CM000684.2:g.20242606T=	GRCh38
NC_000022.10:g.20230129T= , CM000684.1:g.20230129T=	GRCh37
NC_000022.9:g.18610129T=	NCBI36
NG_012176.1:g.30688A=
NG_012176.2:g.30688A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.527A= MANE Select	ENSP00000043402.7:p.Asp176=
ENST00000043402.7:c.527A=	ENSP00000043402.7:p.Asp176=
ENST00000416372.5:c.586A=
ENST00000425986.1:c.784A=
ENST00000469601.1:n.663A=
NM_023004.5:c.527A=	NP_075380.1:p.Asp176=
NM_023004.6:c.527A= MANE Select	NP_075380.1:p.Asp176=