Canonical Allele Identifier: CA2695209279
Gene: RP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54626171_54626181del , CM000670.2:g.54626171_54626181del GRCh38
NC_000008.10:g.55538731_55538741del , CM000670.1:g.55538731_55538741del GRCh37
NC_000008.9:g.55701284_55701294del NCBI36
NG_009840.1:g.15105_15115del
NG_009840.2:g.15105_15115del

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.2289_2299del MANE Select ENSP00000220676.1:p.Asn763LysfsTer14
ENST00000636932.1:c.787+3883_787+3893del ENSP00000489857.1:n.787+3883_787+3893del
ENST00000637698.1:c.787+3883_787+3893del ENSP00000490104.1:n.787+3883_787+3893del
ENST00000220676.1:c.2289_2299del ENSP00000220676.1:p.Asn763LysfsTer14
NM_006269.1:c.2289_2299del NP_006260.1:p.Asn763LysfsTer14
XM_017013721.1:c.2310_2320del XP_016869210.1:p.Asn770LysfsTer14
XM_017013722.1:c.2289_2299del XP_016869211.1:p.Asn763LysfsTer14
NM_001375654.1:c.787+3883_787+3893del NP_001362583.1:n.787+3883_787+3893del
NM_006269.2:c.2289_2299del MANE Select NP_006260.1:p.Asn763LysfsTer14