Canonical Allele Identifier: CA513693414

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230151G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.505C>T MANE Select	ENSP00000043402.7:p.Leu169=
ENST00000043402.7:c.505C>T	ENSP00000043402.7:p.Leu169=
ENST00000416372.5:c.564C>T
ENST00000425986.1:c.762C>T
ENST00000469601.1:n.641C>T
NM_023004.5:c.505C>T	NP_075380.1:p.Leu169=
NM_023004.6:c.505C>T MANE Select	NP_075380.1:p.Leu169=