Canonical Allele Identifier: CA2687301832

Gene: RP1

Linked Data

• gnomAD v4: 8-54626324-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54626325del , CM000670.2:g.54626325del	GRCh38
NC_000008.10:g.55538885del , CM000670.1:g.55538885del	GRCh37
NC_000008.9:g.55701438del	NCBI36
NG_009840.1:g.15259del
NG_009840.2:g.15259del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.2443del MANE Select	ENSP00000220676.1:p.Glu815LysfsTer?
ENST00000636932.1:c.787+4037del	ENSP00000489857.1:n.787+4037del
ENST00000637698.1:c.787+4037del	ENSP00000490104.1:n.787+4037del
ENST00000220676.1:c.2443del	ENSP00000220676.1:p.Glu815LysfsTer?
NM_006269.1:c.2443del	NP_006260.1:p.Glu815LysfsTer?
XM_017013721.1:c.2464del	XP_016869210.1:p.Glu822LysfsTer?
XM_017013722.1:c.2443del	XP_016869211.1:p.Glu815LysfsTer?
NM_001375654.1:c.787+4037del	NP_001362583.1:n.787+4037del
NM_006269.2:c.2443del MANE Select	NP_006260.1:p.Glu815LysfsTer?