Canonical Allele Identifier: CA410712877

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230193C>G (hg19) ; chr22:g.20242670C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242670C>G , CM000684.2:g.20242670C>G	GRCh38
NC_000022.10:g.20230193C>G , CM000684.1:g.20230193C>G	GRCh37
NC_000022.9:g.18610193C>G	NCBI36
NG_012176.1:g.30624G>C
NG_012176.2:g.30624G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.463G>C MANE Select	ENSP00000043402.7:p.Ala155Pro
ENST00000043402.7:c.463G>C	ENSP00000043402.7:p.Ala155Pro
ENST00000416372.5:c.522G>C
ENST00000425986.1:c.720G>C
ENST00000469601.1:n.599G>C
NM_023004.5:c.463G>C	NP_075380.1:p.Ala155Pro
NM_023004.6:c.463G>C MANE Select	NP_075380.1:p.Ala155Pro