Canonical Allele Identifier: CA410712703
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242621T>A , CM000684.2:g.20242621T>A GRCh38
NC_000022.10:g.20230144T>A , CM000684.1:g.20230144T>A GRCh37
NC_000022.9:g.18610144T>A NCBI36
NG_012176.1:g.30673A>T
NG_012176.2:g.30673A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.512A>T MANE Select ENSP00000043402.7:p.Asp171Val
ENST00000043402.7:c.512A>T ENSP00000043402.7:p.Asp171Val
ENST00000416372.5:c.571A>T
ENST00000425986.1:c.769A>T
ENST00000469601.1:n.648A>T
NM_023004.5:c.512A>T NP_075380.1:p.Asp171Val
NM_023004.6:c.512A>T MANE Select NP_075380.1:p.Asp171Val