Canonical Allele Identifier: CA1785189028
Gene: RP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54628093G= , CM000670.2:g.54628093G= GRCh38
NC_000008.10:g.55540653G= , CM000670.1:g.55540653G= GRCh37
NC_000008.9:g.55703206G= NCBI36
NG_009840.1:g.17027G=
NG_009840.2:g.17027G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.4211G= MANE Select ENSP00000220676.1:p.Ser1404=
ENST00000636932.1:c.787+5805G= ENSP00000489857.1:n.787+5805G=
ENST00000637698.1:c.787+5805G= ENSP00000490104.1:n.787+5805G=
ENST00000220676.1:c.4211G= ENSP00000220676.1:p.Ser1404=
NM_006269.1:c.4211G= NP_006260.1:p.Ser1404=
XM_017013721.1:c.4232G= XP_016869210.1:p.Ser1411=
XM_017013722.1:c.4211G= XP_016869211.1:p.Ser1404=
NM_001375654.1:c.787+5805G= NP_001362583.1:n.787+5805G=
NM_006269.2:c.4211G= MANE Select NP_006260.1:p.Ser1404=