Canonical Allele Identifier: CA2396269048
Gene: RTN4R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242416T= , CM000684.2:g.20242416T= GRCh38
NC_000022.10:g.20229939T= , CM000684.1:g.20229939T= GRCh37
NC_000022.9:g.18609939T= NCBI36
NG_012176.1:g.30878A=
NG_012176.2:g.30878A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.717A= MANE Select ENSP00000043402.7:p.Ser239=
ENST00000043402.7:c.717A= ENSP00000043402.7:p.Ser239=
ENST00000416372.5:c.776A=
ENST00000425986.1:c.974A=
NM_023004.5:c.717A= NP_075380.1:p.Ser239=
NM_023004.6:c.717A= MANE Select NP_075380.1:p.Ser239=
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