Canonical Allele Identifier: CA2396269076
Gene: RTN4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20242493C= , CM000684.2:g.20242493C= GRCh38
NC_000022.10:g.20230016C= , CM000684.1:g.20230016C= GRCh37
NC_000022.9:g.18610016C= NCBI36
NG_012176.1:g.30801G=
NG_012176.2:g.30801G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000043402.8:c.640G= MANE Select ENSP00000043402.7:p.Val214=
ENST00000043402.7:c.640G= ENSP00000043402.7:p.Val214=
ENST00000416372.5:c.699G=
ENST00000425986.1:c.897G=
NM_023004.5:c.640G= NP_075380.1:p.Val214=
NM_023004.6:c.640G= MANE Select NP_075380.1:p.Val214=