Canonical Allele Identifier: CA410713251
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242792T>A , CM000684.2:g.20242792T>A GRCh38
NC_000022.10:g.20230315T>A , CM000684.1:g.20230315T>A GRCh37
NC_000022.9:g.18610315T>A NCBI36
NG_012176.1:g.30502A>T
NG_012176.2:g.30502A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000043402.8:c.341A>T MANE Select ENSP00000043402.7:p.Asp114Val
ENST00000043402.7:c.341A>T ENSP00000043402.7:p.Asp114Val
ENST00000416372.5:c.400A>T
ENST00000425986.1:c.598A>T
ENST00000469601.1:n.477A>T
NM_023004.5:c.341A>T NP_075380.1:p.Asp114Val
NM_023004.6:c.341A>T MANE Select NP_075380.1:p.Asp114Val