Canonical Allele Identifier: CA370981011
Gene: RP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54627897T>C , CM000670.2:g.54627897T>C GRCh38
NC_000008.10:g.55540457T>C , CM000670.1:g.55540457T>C GRCh37
NC_000008.9:g.55703010T>C NCBI36
NG_009840.1:g.16831T>C
NG_009840.2:g.16831T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.4015T>C MANE Select ENSP00000220676.1:p.Cys1339Arg
ENST00000636932.1:c.787+5609T>C ENSP00000489857.1:n.787+5609T>C
ENST00000637698.1:c.787+5609T>C ENSP00000490104.1:n.787+5609T>C
ENST00000220676.1:c.4015T>C ENSP00000220676.1:p.Cys1339Arg
NM_006269.1:c.4015T>C NP_006260.1:p.Cys1339Arg
XM_017013721.1:c.4036T>C XP_016869210.1:p.Cys1346Arg
XM_017013722.1:c.4015T>C XP_016869211.1:p.Cys1339Arg
NM_001375654.1:c.787+5609T>C NP_001362583.1:n.787+5609T>C
NM_006269.2:c.4015T>C MANE Select NP_006260.1:p.Cys1339Arg