Canonical Allele Identifier: CA461098722

Gene: RP1

Linked Data

• MyVariant Identifiers: chr8:g.55538638G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54626078G>A , CM000670.2:g.54626078G>A	GRCh38
NC_000008.10:g.55538638G>A , CM000670.1:g.55538638G>A	GRCh37
NC_000008.9:g.55701191G>A	NCBI36
NG_009840.1:g.15012G>A
NG_009840.2:g.15012G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.2196G>A MANE Select	ENSP00000220676.1:p.Gln732=
ENST00000636932.1:c.787+3790G>A	ENSP00000489857.1:n.787+3790G>A
ENST00000637698.1:c.787+3790G>A	ENSP00000490104.1:n.787+3790G>A
ENST00000220676.1:c.2196G>A	ENSP00000220676.1:p.Gln732=
NM_006269.1:c.2196G>A	NP_006260.1:p.Gln732=
XM_017013721.1:c.2217G>A	XP_016869210.1:p.Gln739=
XM_017013722.1:c.2196G>A	XP_016869211.1:p.Gln732=
NM_001375654.1:c.787+3790G>A	NP_001362583.1:n.787+3790G>A
NM_006269.2:c.2196G>A MANE Select	NP_006260.1:p.Gln732=