Canonical Allele Identifier: CA1401209216
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530894_129530896delinsCCT , CM000665.2:g.129530894_129530896delinsCCT GRCh38
NC_000003.11:g.129249737_129249739delinsCCT , CM000665.1:g.129249737_129249739delinsCCT GRCh37
NC_000003.10:g.130732427_130732429delinsCCT NCBI36
NG_009115.1:g.7256_7258delinsCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.380_382delinsCCT MANE Select ENSP00000296271.3:p.Ser127=
ENST00000296271.3:c.380_382delinsCCT ENSP00000296271.3:p.Ser127=
NM_000539.3:c.380_382delinsCCT MANE Select NP_000530.1:p.Ser127=