Canonical Allele Identifier: CA645605457
Gene: RTN4R HGNC NCBI

Linked Data

COSMIC: COSM5057681
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242393del , CM000684.2:g.20242393del GRCh38
NC_000022.10:g.20229916del , CM000684.1:g.20229916del GRCh37
NC_000022.9:g.18609916del NCBI36
NG_012176.1:g.30906del
NG_012176.2:g.30906del

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.745del MANE Select ENSP00000043402.7:p.Leu249CysfsTer7
ENST00000043402.7:c.745del ENSP00000043402.7:p.Leu249CysfsTer7
ENST00000416372.5:c.804del
ENST00000425986.1:c.1002del
NM_023004.5:c.745del NP_075380.1:p.Leu249CysfsTer7
NM_023004.6:c.745del MANE Select NP_075380.1:p.Leu249CysfsTer7
Search 100 bp 5'
Search 100 bp 3'