Canonical Allele Identifier: CA177181644

Gene: RP1

Linked Data

• ClinVar Variation Id: 2838245
• ClinVar RCV Id: RCV003694948
• dbSNP Id: rs769946384
• gnomAD v3: 8-54628168-A-G
• gnomAD v4: 8-54628168-A-G
• MyVariant Identifiers: chr8:g.55540728A>G (hg19) ; chr8:g.54628168A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54628168A>G , CM000670.2:g.54628168A>G	GRCh38
NC_000008.10:g.55540728A>G , CM000670.1:g.55540728A>G	GRCh37
NC_000008.9:g.55703281A>G	NCBI36
NG_009840.1:g.17102A>G
NG_009840.2:g.17102A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.4286A>G MANE Select	ENSP00000220676.1:p.Gln1429Arg
ENST00000636932.1:c.787+5880A>G	ENSP00000489857.1:n.787+5880A>G
ENST00000637698.1:c.787+5880A>G	ENSP00000490104.1:n.787+5880A>G
ENST00000220676.1:c.4286A>G	ENSP00000220676.1:p.Gln1429Arg
NM_006269.1:c.4286A>G	NP_006260.1:p.Gln1429Arg
XM_017013721.1:c.4307A>G	XP_016869210.1:p.Gln1436Arg
XM_017013722.1:c.4286A>G	XP_016869211.1:p.Gln1429Arg
NM_001375654.1:c.787+5880A>G	NP_001362583.1:n.787+5880A>G
NM_006269.2:c.4286A>G MANE Select	NP_006260.1:p.Gln1429Arg