Canonical Allele Identifier: CA177236597

Gene: RP1

Linked Data

• ClinVar Variation Id: 2121727
• ClinVar RCV Id: RCV003043340
• dbSNP Id: rs202098209
• gnomAD v4: 8-54624900-A-G
• MyVariant Identifiers: chr8:g.55537460A>G (hg19) ; chr8:g.54624900A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54624900A>G , CM000670.2:g.54624900A>G	GRCh38
NC_000008.10:g.55537460A>G , CM000670.1:g.55537460A>G	GRCh37
NC_000008.9:g.55700013A>G	NCBI36
NG_009840.1:g.13834A>G
NG_009840.2:g.13834A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000220676.2:c.1018A>G MANE Select	ENSP00000220676.1:p.Arg340Gly
ENST00000636932.1:c.787+2612A>G	ENSP00000489857.1:n.787+2612A>G
ENST00000637698.1:c.787+2612A>G	ENSP00000490104.1:n.787+2612A>G
ENST00000220676.1:c.1018A>G	ENSP00000220676.1:p.Arg340Gly
NM_006269.1:c.1018A>G	NP_006260.1:p.Arg340Gly
XM_017013721.1:c.1039A>G	XP_016869210.1:p.Arg347Gly
XM_017013722.1:c.1018A>G	XP_016869211.1:p.Arg340Gly
NM_001375654.1:c.787+2612A>G	NP_001362583.1:n.787+2612A>G
NM_006269.2:c.1018A>G MANE Select	NP_006260.1:p.Arg340Gly