Canonical Allele Identifier: CA1785188272

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54626329A= , CM000670.2:g.54626329A=	GRCh38
NC_000008.10:g.55538889A= , CM000670.1:g.55538889A=	GRCh37
NC_000008.9:g.55701442A=	NCBI36
NG_009840.1:g.15263A=
NG_009840.2:g.15263A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.2447A= MANE Select	ENSP00000220676.1:p.Asn816=
ENST00000636932.1:c.787+4041A=	ENSP00000489857.1:n.787+4041A=
ENST00000637698.1:c.787+4041A=	ENSP00000490104.1:n.787+4041A=
ENST00000220676.1:c.2447A=	ENSP00000220676.1:p.Asn816=
NM_006269.1:c.2447A=	NP_006260.1:p.Asn816=
XM_017013721.1:c.2468A=	XP_016869210.1:p.Asn823=
XM_017013722.1:c.2447A=	XP_016869211.1:p.Asn816=
NM_001375654.1:c.787+4041A=	NP_001362583.1:n.787+4041A=
NM_006269.2:c.2447A= MANE Select	NP_006260.1:p.Asn816=