Canonical Allele Identifier: CA2695209280

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54626186del , CM000670.2:g.54626186del	GRCh38
NC_000008.10:g.55538746del , CM000670.1:g.55538746del	GRCh37
NC_000008.9:g.55701299del	NCBI36
NG_009840.1:g.15120del
NG_009840.2:g.15120del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.2304del MANE Select	ENSP00000220676.1:p.Lys769ArgfsTer6
ENST00000636932.1:c.787+3898del	ENSP00000489857.1:n.787+3898del
ENST00000637698.1:c.787+3898del	ENSP00000490104.1:n.787+3898del
ENST00000220676.1:c.2304del	ENSP00000220676.1:p.Lys769ArgfsTer6
NM_006269.1:c.2304del	NP_006260.1:p.Lys769ArgfsTer6
XM_017013721.1:c.2325del	XP_016869210.1:p.Lys776ArgfsTer6
XM_017013722.1:c.2304del	XP_016869211.1:p.Lys769ArgfsTer6
NM_001375654.1:c.787+3898del	NP_001362583.1:n.787+3898del
NM_006269.2:c.2304del MANE Select	NP_006260.1:p.Lys769ArgfsTer6