Canonical Allele Identifier: CA513693424

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230152T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242629T>A , CM000684.2:g.20242629T>A	GRCh38
NC_000022.10:g.20230152T>A , CM000684.1:g.20230152T>A	GRCh37
NC_000022.9:g.18610152T>A	NCBI36
NG_012176.1:g.30665A>T
NG_012176.2:g.30665A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.504A>T MANE Select	ENSP00000043402.7:p.Ala168=
ENST00000043402.7:c.504A>T	ENSP00000043402.7:p.Ala168=
ENST00000416372.5:c.563A>T
ENST00000425986.1:c.761A>T
ENST00000469601.1:n.640A>T
NM_023004.5:c.504A>T	NP_075380.1:p.Ala168=
NM_023004.6:c.504A>T MANE Select	NP_075380.1:p.Ala168=