Canonical Allele Identifier: CA370991322
Gene: RP1 HGNC NCBI

Linked Data

dbSNP Id: rs1806019572
gnomAD v4: 8-54625590-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54625590A>G , CM000670.2:g.54625590A>G GRCh38
NC_000008.10:g.55538150A>G , CM000670.1:g.55538150A>G GRCh37
NC_000008.9:g.55700703A>G NCBI36
NG_009840.1:g.14524A>G
NG_009840.2:g.14524A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.1708A>G MANE Select ENSP00000220676.1:p.Ile570Val
ENST00000636932.1:c.787+3302A>G ENSP00000489857.1:n.787+3302A>G
ENST00000637698.1:c.787+3302A>G ENSP00000490104.1:n.787+3302A>G
ENST00000220676.1:c.1708A>G ENSP00000220676.1:p.Ile570Val
NM_006269.1:c.1708A>G NP_006260.1:p.Ile570Val
XM_017013721.1:c.1729A>G XP_016869210.1:p.Ile577Val
XM_017013722.1:c.1708A>G XP_016869211.1:p.Ile570Val
NM_001375654.1:c.787+3302A>G NP_001362583.1:n.787+3302A>G
NM_006269.2:c.1708A>G MANE Select NP_006260.1:p.Ile570Val