Canonical Allele Identifier: CA2687301977
Gene: RP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54627934_54627935insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG , CM000670.2:g.54627934_54627935insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG GRCh38
NC_000008.10:g.55540494_55540495insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG , CM000670.1:g.55540494_55540495insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG GRCh37
NC_000008.9:g.55703047_55703048insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG NCBI36
NG_009840.1:g.16868_16869insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG
NG_009840.2:g.16868_16869insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.4052_4053insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG MANE Select ENSP00000220676.1:p.Tyr1352AlafsTer9
ENST00000636932.1:c.787+5646_787+5647insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG ENSP00000489857.1:n.787+5646_787+5647insGGCCGGGCGCGGTGGCTCACG...
ENST00000637698.1:c.787+5646_787+5647insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG ENSP00000490104.1:n.787+5646_787+5647insGGCCGGGCGCGGTGGCTCACG...
ENST00000220676.1:c.4052_4053insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG ENSP00000220676.1:p.Tyr1352AlafsTer9
NM_006269.1:c.4052_4053insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG NP_006260.1:p.Tyr1352AlafsTer9
XM_017013721.1:c.4073_4074insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG XP_016869210.1:p.Tyr1359AlafsTer9
XM_017013722.1:c.4052_4053insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG XP_016869211.1:p.Tyr1352AlafsTer9
NM_001375654.1:c.787+5646_787+5647insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG NP_001362583.1:n.787+5646_787+5647insGGCCGGGCGCGGTGGCTCACGCCT...
NM_006269.2:c.4052_4053insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG MANE Select NP_006260.1:p.Tyr1352AlafsTer9