Canonical Allele Identifier: CA410712181

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20229919A>T (hg19) ; chr22:g.20242396A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242396A>T , CM000684.2:g.20242396A>T	GRCh38
NC_000022.10:g.20229919A>T , CM000684.1:g.20229919A>T	GRCh37
NC_000022.9:g.18609919A>T	NCBI36
NG_012176.1:g.30898T>A
NG_012176.2:g.30898T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.737T>A MANE Select	ENSP00000043402.7:p.Leu246Gln
ENST00000043402.7:c.737T>A	ENSP00000043402.7:p.Leu246Gln
ENST00000416372.5:c.796T>A
ENST00000425986.1:c.994T>A
NM_023004.5:c.737T>A	NP_075380.1:p.Leu246Gln
NM_023004.6:c.737T>A MANE Select	NP_075380.1:p.Leu246Gln