Canonical Allele Identifier: CA410712165
Gene: RTN4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242387A>T , CM000684.2:g.20242387A>T GRCh38
NC_000022.10:g.20229910A>T , CM000684.1:g.20229910A>T GRCh37
NC_000022.9:g.18609910A>T NCBI36
NG_012176.1:g.30907T>A
NG_012176.2:g.30907T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.746T>A MANE Select ENSP00000043402.7:p.Leu249Gln
ENST00000043402.7:c.746T>A ENSP00000043402.7:p.Leu249Gln
ENST00000416372.5:c.805T>A
ENST00000425986.1:c.1003T>A
NM_023004.5:c.746T>A NP_075380.1:p.Leu249Gln
NM_023004.6:c.746T>A MANE Select NP_075380.1:p.Leu249Gln