Canonical Allele Identifier: CA4751741
Gene: RP1 HGNC NCBI

Linked Data

dbSNP Id: rs760506749
gnomAD v2: 8-55540194-T-G
gnomAD v4: 8-54627634-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.54627634T>G , CM000670.2:g.54627634T>G GRCh38
NC_000008.10:g.55540194T>G , CM000670.1:g.55540194T>G GRCh37
NC_000008.9:g.55702747T>G NCBI36
NG_009840.1:g.16568T>G
NG_009840.2:g.16568T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220676.2:c.3752T>G MANE Select ENSP00000220676.1:p.Val1251Gly
ENST00000636932.1:c.787+5346T>G ENSP00000489857.1:n.787+5346T>G
ENST00000637698.1:c.787+5346T>G ENSP00000490104.1:n.787+5346T>G
ENST00000220676.1:c.3752T>G ENSP00000220676.1:p.Val1251Gly
NM_006269.1:c.3752T>G NP_006260.1:p.Val1251Gly
XM_017013721.1:c.3773T>G XP_016869210.1:p.Val1258Gly
XM_017013722.1:c.3752T>G XP_016869211.1:p.Val1251Gly
NM_001375654.1:c.787+5346T>G NP_001362583.1:n.787+5346T>G
NM_006269.2:c.3752T>G MANE Select NP_006260.1:p.Val1251Gly