Canonical Allele Identifier: CA461100088

Gene: RP1

Linked Data

• gnomAD v4: 8-54628187-T-G
• MyVariant Identifiers: chr8:g.55540747T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54628187T>G , CM000670.2:g.54628187T>G	GRCh38
NC_000008.10:g.55540747T>G , CM000670.1:g.55540747T>G	GRCh37
NC_000008.9:g.55703300T>G	NCBI36
NG_009840.1:g.17121T>G
NG_009840.2:g.17121T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.4305T>G MANE Select	ENSP00000220676.1:p.Thr1435=
ENST00000636932.1:c.787+5899T>G	ENSP00000489857.1:n.787+5899T>G
ENST00000637698.1:c.787+5899T>G	ENSP00000490104.1:n.787+5899T>G
ENST00000220676.1:c.4305T>G	ENSP00000220676.1:p.Thr1435=
NM_006269.1:c.4305T>G	NP_006260.1:p.Thr1435=
XM_017013721.1:c.4326T>G	XP_016869210.1:p.Thr1442=
XM_017013722.1:c.4305T>G	XP_016869211.1:p.Thr1435=
NM_001375654.1:c.787+5899T>G	NP_001362583.1:n.787+5899T>G
NM_006269.2:c.4305T>G MANE Select	NP_006260.1:p.Thr1435=