Canonical Allele Identifier: CA461100197
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1111045
ClinVar RCV Id: RCV001437482
dbSNP Id: rs1321915339
gnomAD v2: 8-55540789-C-G
gnomAD v3: 8-54628229-C-G
gnomAD v4: 8-54628229-C-G
MyVariant Identifiers: chr8:g.55540789C>G (hg19) chr8:g.54628229C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54628229C>G , CM000670.2:g.54628229C>G GRCh38
NC_000008.10:g.55540789C>G , CM000670.1:g.55540789C>G GRCh37
NC_000008.9:g.55703342C>G NCBI36
NG_009840.1:g.17163C>G
NG_009840.2:g.17163C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.4347C>G MANE Select ENSP00000220676.1:p.Gly1449=
ENST00000636932.1:c.787+5941C>G ENSP00000489857.1:n.787+5941C>G
ENST00000637698.1:c.787+5941C>G ENSP00000490104.1:n.787+5941C>G
ENST00000220676.1:c.4347C>G ENSP00000220676.1:p.Gly1449=
NM_006269.1:c.4347C>G NP_006260.1:p.Gly1449=
XM_017013721.1:c.4368C>G XP_016869210.1:p.Gly1456=
XM_017013722.1:c.4347C>G XP_016869211.1:p.Gly1449=
NM_001375654.1:c.787+5941C>G NP_001362583.1:n.787+5941C>G
NM_006269.2:c.4347C>G MANE Select NP_006260.1:p.Gly1449=
Search 100 bp 5'
Search 100 bp 3'