Canonical Allele Identifier: CA410712252

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20229954A>T (hg19) ; chr22:g.20242431A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242431A>T , CM000684.2:g.20242431A>T	GRCh38
NC_000022.10:g.20229954A>T , CM000684.1:g.20229954A>T	GRCh37
NC_000022.9:g.18609954A>T	NCBI36
NG_012176.1:g.30863T>A
NG_012176.2:g.30863T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.702T>A MANE Select	ENSP00000043402.7:p.Phe234Leu
ENST00000043402.7:c.702T>A	ENSP00000043402.7:p.Phe234Leu
ENST00000416372.5:c.761T>A
ENST00000425986.1:c.959T>A
NM_023004.5:c.702T>A	NP_075380.1:p.Phe234Leu
NM_023004.6:c.702T>A MANE Select	NP_075380.1:p.Phe234Leu