Canonical Allele Identifier: CA370981285

Gene: RP1

Linked Data

• ClinVar Variation Id: 958232
• ClinVar RCV Id: RCV001231353
• dbSNP Id: rs1806122778
• MyVariant Identifiers: chr8:g.55540551A>T (hg19) ; chr8:g.54627991A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54627991A>T , CM000670.2:g.54627991A>T	GRCh38
NC_000008.10:g.55540551A>T , CM000670.1:g.55540551A>T	GRCh37
NC_000008.9:g.55703104A>T	NCBI36
NG_009840.1:g.16925A>T
NG_009840.2:g.16925A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000220676.2:c.4109A>T MANE Select	ENSP00000220676.1:p.Lys1370Ile
ENST00000636932.1:c.787+5703A>T	ENSP00000489857.1:n.787+5703A>T
ENST00000637698.1:c.787+5703A>T	ENSP00000490104.1:n.787+5703A>T
ENST00000220676.1:c.4109A>T	ENSP00000220676.1:p.Lys1370Ile
NM_006269.1:c.4109A>T	NP_006260.1:p.Lys1370Ile
XM_017013721.1:c.4130A>T	XP_016869210.1:p.Lys1377Ile
XM_017013722.1:c.4109A>T	XP_016869211.1:p.Lys1370Ile
NM_001375654.1:c.787+5703A>T	NP_001362583.1:n.787+5703A>T
NM_006269.2:c.4109A>T MANE Select	NP_006260.1:p.Lys1370Ile