Canonical Allele Identifier: CA461100669

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54629679C>A , CM000670.2:g.54629679C>A	GRCh38
NC_000008.10:g.55542239C>A , CM000670.1:g.55542239C>A	GRCh37
NC_000008.9:g.55704792C>A	NCBI36
NG_009840.1:g.18613C>A
NG_009840.2:g.18613C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006269.2:c.5797C>A MANE Select	NP_006260.1:p.Arg1933=
ENST00000220676.2:c.5797C>A MANE Select	ENSP00000220676.1:p.Arg1933=
NM_001375654.1:c.787+7391C>A	NP_001362583.1:n.787+7391C>A
NM_006269.1:c.5797C>A	NP_006260.1:p.Arg1933=
ENST00000220676.1:c.5797C>A	ENSP00000220676.1:p.Arg1933=
ENST00000636932.1:c.787+7391C>A	ENSP00000489857.1:n.787+7391C>A
ENST00000637698.1:c.787+7391C>A	ENSP00000490104.1:n.787+7391C>A
XM_017013721.1:c.5818C>A	XP_016869210.1:p.Arg1940=
XM_017013722.1:c.5797C>A	XP_016869211.1:p.Arg1933=