Canonical Allele Identifier: CA2396269057
Gene: RTN4R HGNC NCBI

Linked Data

dbSNP Id: rs2051113664
gnomAD v4: 22-20242434-CAGAT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242438_20242441del , CM000684.2:g.20242438_20242441del GRCh38
NC_000022.10:g.20229961_20229964del , CM000684.1:g.20229961_20229964del GRCh37
NC_000022.9:g.18609961_18609964del NCBI36
NG_012176.1:g.30856_30859del
NG_012176.2:g.30856_30859del

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.695_698del MANE Select ENSP00000043402.7:p.Tyr232CysfsTer23
ENST00000043402.7:c.695_698del ENSP00000043402.7:p.Tyr232CysfsTer23
ENST00000416372.5:c.754_757del
ENST00000425986.1:c.952_955del
NM_023004.5:c.695_698del NP_075380.1:p.Tyr232CysfsTer23
NM_023004.6:c.695_698del MANE Select NP_075380.1:p.Tyr232CysfsTer23
Search 100 bp 5'
Search 100 bp 3'