Canonical Allele Identifier: CA370980768

Gene: RP1

Linked Data

• ClinVar Variation Id: 1436289
• ClinVar RCV Id: RCV002002062
• dbSNP Id: rs2129317379
• MyVariant Identifiers: chr8:g.55540386G>A (hg19) ; chr8:g.54627826G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54627826G>A , CM000670.2:g.54627826G>A	GRCh38
NC_000008.10:g.55540386G>A , CM000670.1:g.55540386G>A	GRCh37
NC_000008.9:g.55702939G>A	NCBI36
NG_009840.1:g.16760G>A
NG_009840.2:g.16760G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.3944G>A MANE Select	ENSP00000220676.1:p.Cys1315Tyr
ENST00000636932.1:c.787+5538G>A	ENSP00000489857.1:n.787+5538G>A
ENST00000637698.1:c.787+5538G>A	ENSP00000490104.1:n.787+5538G>A
ENST00000220676.1:c.3944G>A	ENSP00000220676.1:p.Cys1315Tyr
NM_006269.1:c.3944G>A	NP_006260.1:p.Cys1315Tyr
XM_017013721.1:c.3965G>A	XP_016869210.1:p.Cys1322Tyr
XM_017013722.1:c.3944G>A	XP_016869211.1:p.Cys1315Tyr
NM_001375654.1:c.787+5538G>A	NP_001362583.1:n.787+5538G>A
NM_006269.2:c.3944G>A MANE Select	NP_006260.1:p.Cys1315Tyr