Canonical Allele Identifier: CA370993333
Gene: RP1 HGNC NCBI

Linked Data

dbSNP Id: rs1184391962
gnomAD v4: 8-54626170-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54626170A>C , CM000670.2:g.54626170A>C GRCh38
NC_000008.10:g.55538730A>C , CM000670.1:g.55538730A>C GRCh37
NC_000008.9:g.55701283A>C NCBI36
NG_009840.1:g.15104A>C
NG_009840.2:g.15104A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.2288A>C MANE Select ENSP00000220676.1:p.Asn763Thr
ENST00000636932.1:c.787+3882A>C ENSP00000489857.1:n.787+3882A>C
ENST00000637698.1:c.787+3882A>C ENSP00000490104.1:n.787+3882A>C
ENST00000220676.1:c.2288A>C ENSP00000220676.1:p.Asn763Thr
NM_006269.1:c.2288A>C NP_006260.1:p.Asn763Thr
XM_017013721.1:c.2309A>C XP_016869210.1:p.Asn770Thr
XM_017013722.1:c.2288A>C XP_016869211.1:p.Asn763Thr
NM_001375654.1:c.787+3882A>C NP_001362583.1:n.787+3882A>C
NM_006269.2:c.2288A>C MANE Select NP_006260.1:p.Asn763Thr