Canonical Allele Identifier: CA370981000

Gene: RP1

Linked Data

• ClinVar Variation Id: 1472399
• ClinVar RCV Id: RCV001975992 ; RCV002571333
• dbSNP Id: rs746414248
• gnomAD v2: 8-55540455-T-A
• gnomAD v4: 8-54627895-T-A
• MyVariant Identifiers: chr8:g.55540455T>A (hg19) ; chr8:g.54627895T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54627895T>A , CM000670.2:g.54627895T>A	GRCh38
NC_000008.10:g.55540455T>A , CM000670.1:g.55540455T>A	GRCh37
NC_000008.9:g.55703008T>A	NCBI36
NG_009840.1:g.16829T>A
NG_009840.2:g.16829T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.4013T>A MANE Select	ENSP00000220676.1:p.Val1338Asp
ENST00000636932.1:c.787+5607T>A	ENSP00000489857.1:n.787+5607T>A
ENST00000637698.1:c.787+5607T>A	ENSP00000490104.1:n.787+5607T>A
ENST00000220676.1:c.4013T>A	ENSP00000220676.1:p.Val1338Asp
NM_006269.1:c.4013T>A	NP_006260.1:p.Val1338Asp
XM_017013721.1:c.4034T>A	XP_016869210.1:p.Val1345Asp
XM_017013722.1:c.4013T>A	XP_016869211.1:p.Val1338Asp
NM_001375654.1:c.787+5607T>A	NP_001362583.1:n.787+5607T>A
NM_006269.2:c.4013T>A MANE Select	NP_006260.1:p.Val1338Asp