Canonical Allele Identifier: CA461099522

Gene: RP1

Linked Data

• MyVariant Identifiers: chr8:g.55540390T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54627830T>A , CM000670.2:g.54627830T>A	GRCh38
NC_000008.10:g.55540390T>A , CM000670.1:g.55540390T>A	GRCh37
NC_000008.9:g.55702943T>A	NCBI36
NG_009840.1:g.16764T>A
NG_009840.2:g.16764T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.3948T>A MANE Select	ENSP00000220676.1:p.Ala1316=
ENST00000636932.1:c.787+5542T>A	ENSP00000489857.1:n.787+5542T>A
ENST00000637698.1:c.787+5542T>A	ENSP00000490104.1:n.787+5542T>A
ENST00000220676.1:c.3948T>A	ENSP00000220676.1:p.Ala1316=
NM_006269.1:c.3948T>A	NP_006260.1:p.Ala1316=
XM_017013721.1:c.3969T>A	XP_016869210.1:p.Ala1323=
XM_017013722.1:c.3948T>A	XP_016869211.1:p.Ala1316=
NM_001375654.1:c.787+5542T>A	NP_001362583.1:n.787+5542T>A
NM_006269.2:c.3948T>A MANE Select	NP_006260.1:p.Ala1316=