Canonical Allele Identifier: CA370992608

Gene: RP1

Linked Data

• ClinVar Variation Id: 1443466
• ClinVar RCV Id: RCV001955617
• dbSNP Id: rs2129316399
• MyVariant Identifiers: chr8:g.55538489T>A (hg19) ; chr8:g.54625929T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54625929T>A , CM000670.2:g.54625929T>A	GRCh38
NC_000008.10:g.55538489T>A , CM000670.1:g.55538489T>A	GRCh37
NC_000008.9:g.55701042T>A	NCBI36
NG_009840.1:g.14863T>A
NG_009840.2:g.14863T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220676.2:c.2047T>A MANE Select	ENSP00000220676.1:p.Ser683Thr
ENST00000636932.1:c.787+3641T>A	ENSP00000489857.1:n.787+3641T>A
ENST00000637698.1:c.787+3641T>A	ENSP00000490104.1:n.787+3641T>A
ENST00000220676.1:c.2047T>A	ENSP00000220676.1:p.Ser683Thr
NM_006269.1:c.2047T>A	NP_006260.1:p.Ser683Thr
XM_017013721.1:c.2068T>A	XP_016869210.1:p.Ser690Thr
XM_017013722.1:c.2047T>A	XP_016869211.1:p.Ser683Thr
NM_001375654.1:c.787+3641T>A	NP_001362583.1:n.787+3641T>A
NM_006269.2:c.2047T>A MANE Select	NP_006260.1:p.Ser683Thr