Canonical Allele Identifier: CA513693469

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230170C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242647C>T , CM000684.2:g.20242647C>T	GRCh38
NC_000022.10:g.20230170C>T , CM000684.1:g.20230170C>T	GRCh37
NC_000022.9:g.18610170C>T	NCBI36
NG_012176.1:g.30647G>A
NG_012176.2:g.30647G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.486G>A MANE Select	ENSP00000043402.7:p.Gln162=
ENST00000043402.7:c.486G>A	ENSP00000043402.7:p.Gln162=
ENST00000416372.5:c.545G>A
ENST00000425986.1:c.743G>A
ENST00000469601.1:n.622G>A
NM_023004.5:c.486G>A	NP_075380.1:p.Gln162=
NM_023004.6:c.486G>A MANE Select	NP_075380.1:p.Gln162=