Canonical Allele Identifier: CA410712726

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230151G>T (hg19) ; chr22:g.20242628G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242628G>T , CM000684.2:g.20242628G>T	GRCh38
NC_000022.10:g.20230151G>T , CM000684.1:g.20230151G>T	GRCh37
NC_000022.9:g.18610151G>T	NCBI36
NG_012176.1:g.30666C>A
NG_012176.2:g.30666C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.505C>A MANE Select	ENSP00000043402.7:p.Leu169Met
ENST00000043402.7:c.505C>A	ENSP00000043402.7:p.Leu169Met
ENST00000416372.5:c.564C>A
ENST00000425986.1:c.762C>A
ENST00000469601.1:n.641C>A
NM_023004.5:c.505C>A	NP_075380.1:p.Leu169Met
NM_023004.6:c.505C>A MANE Select	NP_075380.1:p.Leu169Met