Canonical Allele Identifier: CA4751475
Gene: RP1 HGNC NCBI

Linked Data

dbSNP Id: rs778260802
gnomAD v2: 8-55538505-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54625945G>A , CM000670.2:g.54625945G>A GRCh38
NC_000008.10:g.55538505G>A , CM000670.1:g.55538505G>A GRCh37
NC_000008.9:g.55701058G>A NCBI36
NG_009840.1:g.14879G>A
NG_009840.2:g.14879G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.2063G>A MANE Select ENSP00000220676.1:p.Gly688Glu
ENST00000636932.1:c.787+3657G>A ENSP00000489857.1:n.787+3657G>A
ENST00000637698.1:c.787+3657G>A ENSP00000490104.1:n.787+3657G>A
ENST00000220676.1:c.2063G>A ENSP00000220676.1:p.Gly688Glu
NM_006269.1:c.2063G>A NP_006260.1:p.Gly688Glu
XM_017013721.1:c.2084G>A XP_016869210.1:p.Gly695Glu
XM_017013722.1:c.2063G>A XP_016869211.1:p.Gly688Glu
NM_001375654.1:c.787+3657G>A NP_001362583.1:n.787+3657G>A
NM_006269.2:c.2063G>A MANE Select NP_006260.1:p.Gly688Glu