Canonical Allele Identifier: CA410712649

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230129T>G (hg19) ; chr22:g.20242606T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.527A>C MANE Select	ENSP00000043402.7:p.Asp176Ala
ENST00000043402.7:c.527A>C	ENSP00000043402.7:p.Asp176Ala
ENST00000416372.5:c.586A>C
ENST00000425986.1:c.784A>C
ENST00000469601.1:n.663A>C
NM_023004.5:c.527A>C	NP_075380.1:p.Asp176Ala
NM_023004.6:c.527A>C MANE Select	NP_075380.1:p.Asp176Ala