Canonical Allele Identifier: CA513693444

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230160G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242637G>A , CM000684.2:g.20242637G>A	GRCh38
NC_000022.10:g.20230160G>A , CM000684.1:g.20230160G>A	GRCh37
NC_000022.9:g.18610160G>A	NCBI36
NG_012176.1:g.30657C>T
NG_012176.2:g.30657C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.496C>T MANE Select	ENSP00000043402.7:p.Leu166=
ENST00000043402.7:c.496C>T	ENSP00000043402.7:p.Leu166=
ENST00000416372.5:c.555C>T
ENST00000425986.1:c.753C>T
ENST00000469601.1:n.632C>T
NM_023004.5:c.496C>T	NP_075380.1:p.Leu166=
NM_023004.6:c.496C>T MANE Select	NP_075380.1:p.Leu166=