Canonical Allele Identifier: CA4751776

Gene: RP1

Linked Data

• dbSNP Id: rs768237139
• ExAC: 8:55540392 A / G
• gnomAD v2: 8-55540392-A-G
• gnomAD v4: 8-54627832-A-G
• MyVariant Identifiers: chr8:g.55540392A>G (hg19) ; chr8:g.54627832A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54627832A>G , CM000670.2:g.54627832A>G	GRCh38
NC_000008.10:g.55540392A>G , CM000670.1:g.55540392A>G	GRCh37
NC_000008.9:g.55702945A>G	NCBI36
NG_009840.1:g.16766A>G
NG_009840.2:g.16766A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.3950A>G MANE Select	ENSP00000220676.1:p.Gln1317Arg
ENST00000636932.1:c.787+5544A>G	ENSP00000489857.1:n.787+5544A>G
ENST00000637698.1:c.787+5544A>G	ENSP00000490104.1:n.787+5544A>G
ENST00000220676.1:c.3950A>G	ENSP00000220676.1:p.Gln1317Arg
NM_006269.1:c.3950A>G	NP_006260.1:p.Gln1317Arg
XM_017013721.1:c.3971A>G	XP_016869210.1:p.Gln1324Arg
XM_017013722.1:c.3950A>G	XP_016869211.1:p.Gln1317Arg
NM_001375654.1:c.787+5544A>G	NP_001362583.1:n.787+5544A>G
NM_006269.2:c.3950A>G MANE Select	NP_006260.1:p.Gln1317Arg