Canonical Allele Identifier: CA410712856

Gene: RTN4R

Linked Data

• MyVariant Identifiers: chr22:g.20230187G>A (hg19) ; chr22:g.20242664G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20242664G>A , CM000684.2:g.20242664G>A	GRCh38
NC_000022.10:g.20230187G>A , CM000684.1:g.20230187G>A	GRCh37
NC_000022.9:g.18610187G>A	NCBI36
NG_012176.1:g.30630C>T
NG_012176.2:g.30630C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000043402.8:c.469C>T MANE Select	ENSP00000043402.7:p.Gln157Ter
ENST00000043402.7:c.469C>T	ENSP00000043402.7:p.Gln157Ter
ENST00000416372.5:c.528C>T
ENST00000425986.1:c.726C>T
ENST00000469601.1:n.605C>T
NM_023004.5:c.469C>T	NP_075380.1:p.Gln157Ter
NM_023004.6:c.469C>T MANE Select	NP_075380.1:p.Gln157Ter