Canonical Allele Identifier: CA1785188372

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54626542A= , CM000670.2:g.54626542A=	GRCh38
NC_000008.10:g.55539102A= , CM000670.1:g.55539102A=	GRCh37
NC_000008.9:g.55701655A=	NCBI36
NG_009840.1:g.15476A=
NG_009840.2:g.15476A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.2660A= MANE Select	ENSP00000220676.1:p.His887=
ENST00000636932.1:c.787+4254A=	ENSP00000489857.1:n.787+4254A=
ENST00000637698.1:c.787+4254A=	ENSP00000490104.1:n.787+4254A=
ENST00000220676.1:c.2660A=	ENSP00000220676.1:p.His887=
NM_006269.1:c.2660A=	NP_006260.1:p.His887=
XM_017013721.1:c.2681A=	XP_016869210.1:p.His894=
XM_017013722.1:c.2660A=	XP_016869211.1:p.His887=
NM_001375654.1:c.787+4254A=	NP_001362583.1:n.787+4254A=
NM_006269.2:c.2660A= MANE Select	NP_006260.1:p.His887=