Canonical Allele Identifier: CA461099833

Gene: RP1

Linked Data

• gnomAD v4: 8-54627935-A-C
• MyVariant Identifiers: chr8:g.55540495A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54627935A>C , CM000670.2:g.54627935A>C	GRCh38
NC_000008.10:g.55540495A>C , CM000670.1:g.55540495A>C	GRCh37
NC_000008.9:g.55703048A>C	NCBI36
NG_009840.1:g.16869A>C
NG_009840.2:g.16869A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.4053A>C MANE Select	ENSP00000220676.1:p.Thr1351=
ENST00000636932.1:c.787+5647A>C	ENSP00000489857.1:n.787+5647A>C
ENST00000637698.1:c.787+5647A>C	ENSP00000490104.1:n.787+5647A>C
ENST00000220676.1:c.4053A>C	ENSP00000220676.1:p.Thr1351=
NM_006269.1:c.4053A>C	NP_006260.1:p.Thr1351=
XM_017013721.1:c.4074A>C	XP_016869210.1:p.Thr1358=
XM_017013722.1:c.4053A>C	XP_016869211.1:p.Thr1351=
NM_001375654.1:c.787+5647A>C	NP_001362583.1:n.787+5647A>C
NM_006269.2:c.4053A>C MANE Select	NP_006260.1:p.Thr1351=