Canonical Allele Identifier: CA1401208267
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530531_129530535delinsACAAC , CM000665.2:g.129530531_129530535delinsACAAC GRCh38
NC_000003.11:g.129249374_129249378delinsACAAC , CM000665.1:g.129249374_129249378delinsACAAC GRCh37
NC_000003.10:g.130732064_130732068delinsACAAC NCBI36
NG_009115.1:g.6893_6897delinsACAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-345_362-341delinsACAAC MANE Select ENSP00000296271.3:n.362-345_362-341delinsACAAC
ENST00000296271.3:c.362-345_362-341delinsACAAC ENSP00000296271.3:n.362-345_362-341delinsACAAC
NM_000539.3:c.362-345_362-341delinsACAAC MANE Select NP_000530.1:n.362-345_362-341delinsACAAC