Canonical Allele Identifier: CA370992774

Gene: RP1

Linked Data

• ClinVar Variation Id: 1487942
• ClinVar RCV Id: RCV002008955
• dbSNP Id: rs2129316439
• MyVariant Identifiers: chr8:g.55538562G>A (hg19) ; chr8:g.54626002G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54626002G>A , CM000670.2:g.54626002G>A	GRCh38
NC_000008.10:g.55538562G>A , CM000670.1:g.55538562G>A	GRCh37
NC_000008.9:g.55701115G>A	NCBI36
NG_009840.1:g.14936G>A
NG_009840.2:g.14936G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.2120G>A MANE Select	ENSP00000220676.1:p.Arg707Lys
ENST00000636932.1:c.787+3714G>A	ENSP00000489857.1:n.787+3714G>A
ENST00000637698.1:c.787+3714G>A	ENSP00000490104.1:n.787+3714G>A
ENST00000220676.1:c.2120G>A	ENSP00000220676.1:p.Arg707Lys
NM_006269.1:c.2120G>A	NP_006260.1:p.Arg707Lys
XM_017013721.1:c.2141G>A	XP_016869210.1:p.Arg714Lys
XM_017013722.1:c.2120G>A	XP_016869211.1:p.Arg707Lys
NM_001375654.1:c.787+3714G>A	NP_001362583.1:n.787+3714G>A
NM_006269.2:c.2120G>A MANE Select	NP_006260.1:p.Arg707Lys