Canonical Allele Identifier: CA2396269056
Gene: RTN4R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242434_20242438delinsCAGAT , CM000684.2:g.20242434_20242438delinsCAGAT GRCh38
NC_000022.10:g.20229957_20229961delinsCAGAT , CM000684.1:g.20229957_20229961delinsCAGAT GRCh37
NC_000022.9:g.18609957_18609961delinsCAGAT NCBI36
NG_012176.1:g.30856_30860delinsATCTG
NG_012176.2:g.30856_30860delinsATCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.695_699delinsATCTG MANE Select ENSP00000043402.7:p.Tyr232=
ENST00000043402.7:c.695_699delinsATCTG ENSP00000043402.7:p.Tyr232=
ENST00000416372.5:c.754_758delinsATCTG
ENST00000425986.1:c.952_956delinsATCTG
NM_023004.5:c.695_699delinsATCTG NP_075380.1:p.Tyr232=
NM_023004.6:c.695_699delinsATCTG MANE Select NP_075380.1:p.Tyr232=
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