Canonical Allele Identifier: CA2695209286
Gene: RP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54626316del , CM000670.2:g.54626316del GRCh38
NC_000008.10:g.55538876del , CM000670.1:g.55538876del GRCh37
NC_000008.9:g.55701429del NCBI36
NG_009840.1:g.15250del
NG_009840.2:g.15250del

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.2434del MANE Select ENSP00000220676.1:p.Ser812ValfsTer?
ENST00000636932.1:c.787+4028del ENSP00000489857.1:n.787+4028del
ENST00000637698.1:c.787+4028del ENSP00000490104.1:n.787+4028del
ENST00000220676.1:c.2434del ENSP00000220676.1:p.Ser812ValfsTer?
NM_006269.1:c.2434del NP_006260.1:p.Ser812ValfsTer?
XM_017013721.1:c.2455del XP_016869210.1:p.Ser819ValfsTer?
XM_017013722.1:c.2434del XP_016869211.1:p.Ser812ValfsTer?
NM_001375654.1:c.787+4028del NP_001362583.1:n.787+4028del
NM_006269.2:c.2434del MANE Select NP_006260.1:p.Ser812ValfsTer?