Canonical Allele Identifier: CA370991372

Gene: RP1

Linked Data

• ClinVar Variation Id: 866177
• ClinVar RCV Id: RCV001073978
• dbSNP Id: rs1806020324
• MyVariant Identifiers: chr8:g.55538163C>G (hg19) ; chr8:g.54625603C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54625603C>G , CM000670.2:g.54625603C>G	GRCh38
NC_000008.10:g.55538163C>G , CM000670.1:g.55538163C>G	GRCh37
NC_000008.9:g.55700716C>G	NCBI36
NG_009840.1:g.14537C>G
NG_009840.2:g.14537C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.1721C>G MANE Select	ENSP00000220676.1:p.Ser574Ter
ENST00000636932.1:c.787+3315C>G	ENSP00000489857.1:n.787+3315C>G
ENST00000637698.1:c.787+3315C>G	ENSP00000490104.1:n.787+3315C>G
ENST00000220676.1:c.1721C>G	ENSP00000220676.1:p.Ser574Ter
NM_006269.1:c.1721C>G	NP_006260.1:p.Ser574Ter
XM_017013721.1:c.1742C>G	XP_016869210.1:p.Ser581Ter
XM_017013722.1:c.1721C>G	XP_016869211.1:p.Ser574Ter
NM_001375654.1:c.787+3315C>G	NP_001362583.1:n.787+3315C>G
NM_006269.2:c.1721C>G MANE Select	NP_006260.1:p.Ser574Ter