Canonical Allele Identifier: CA1785188086
Gene: RP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54625921C= , CM000670.2:g.54625921C= GRCh38
NC_000008.10:g.55538481C= , CM000670.1:g.55538481C= GRCh37
NC_000008.9:g.55701034C= NCBI36
NG_009840.1:g.14855C=
NG_009840.2:g.14855C=

Transcript Alleles

HGVS Amino-acid change
ENST00000220676.2:c.2039C= MANE Select ENSP00000220676.1:p.Ala680=
ENST00000636932.1:c.787+3633C= ENSP00000489857.1:n.787+3633C=
ENST00000637698.1:c.787+3633C= ENSP00000490104.1:n.787+3633C=
ENST00000220676.1:c.2039C= ENSP00000220676.1:p.Ala680=
NM_006269.1:c.2039C= NP_006260.1:p.Ala680=
XM_017013721.1:c.2060C= XP_016869210.1:p.Ala687=
XM_017013722.1:c.2039C= XP_016869211.1:p.Ala680=
NM_001375654.1:c.787+3633C= NP_001362583.1:n.787+3633C=
NM_006269.2:c.2039C= MANE Select NP_006260.1:p.Ala680=