Canonical Allele Identifier: CA2780387051
Gene: RP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54627980del , CM000670.2:g.54627980del GRCh38
NC_000008.10:g.55540540del , CM000670.1:g.55540540del GRCh37
NC_000008.9:g.55703093del NCBI36
NG_009840.1:g.16914del
NG_009840.2:g.16914del

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.4098del MANE Select ENSP00000220676.1:p.Asp1366GlufsTer7
ENST00000636932.1:c.787+5692del ENSP00000489857.1:n.787+5692del
ENST00000637698.1:c.787+5692del ENSP00000490104.1:n.787+5692del
ENST00000220676.1:c.4098del ENSP00000220676.1:p.Asp1366GlufsTer7
NM_006269.1:c.4098del NP_006260.1:p.Asp1366GlufsTer7
XM_017013721.1:c.4119del XP_016869210.1:p.Asp1373GlufsTer7
XM_017013722.1:c.4098del XP_016869211.1:p.Asp1366GlufsTer7
NM_001375654.1:c.787+5692del NP_001362583.1:n.787+5692del
NM_006269.2:c.4098del MANE Select NP_006260.1:p.Asp1366GlufsTer7