Canonical Allele Identifier: CA370982710
Community Standard Title: NM_006269.2(RP1):c.4576G>T (p.Glu1526Ter)
Gene: RP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54628458G>T , CM000670.2:g.54628458G>T GRCh38
NC_000008.10:g.55541018G>T , CM000670.1:g.55541018G>T GRCh37
NC_000008.9:g.55703571G>T NCBI36
NG_009840.1:g.17392G>T
NG_009840.2:g.17392G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006269.2:c.4576G>T MANE Select NP_006260.1:p.Glu1526Ter
ENST00000220676.2:c.4576G>T MANE Select ENSP00000220676.1:p.Glu1526Ter
NM_001375654.1:c.787+6170G>T NP_001362583.1:n.787+6170G>T
NM_006269.1:c.4576G>T NP_006260.1:p.Glu1526Ter
ENST00000220676.1:c.4576G>T ENSP00000220676.1:p.Glu1526Ter
ENST00000636932.1:c.787+6170G>T ENSP00000489857.1:n.787+6170G>T
ENST00000637698.1:c.787+6170G>T ENSP00000490104.1:n.787+6170G>T
XM_017013721.1:c.4597G>T XP_016869210.1:p.Glu1533Ter
XM_017013722.1:c.4576G>T XP_016869211.1:p.Glu1526Ter