Canonical Allele Identifier: CA1785188974

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54627981G= , CM000670.2:g.54627981G=	GRCh38
NC_000008.10:g.55540541G= , CM000670.1:g.55540541G=	GRCh37
NC_000008.9:g.55703094G=	NCBI36
NG_009840.1:g.16915G=
NG_009840.2:g.16915G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220676.2:c.4099G= MANE Select	ENSP00000220676.1:p.Asp1367=
ENST00000636932.1:c.787+5693G=	ENSP00000489857.1:n.787+5693G=
ENST00000637698.1:c.787+5693G=	ENSP00000490104.1:n.787+5693G=
ENST00000220676.1:c.4099G=	ENSP00000220676.1:p.Asp1367=
NM_006269.1:c.4099G=	NP_006260.1:p.Asp1367=
XM_017013721.1:c.4120G=	XP_016869210.1:p.Asp1374=
XM_017013722.1:c.4099G=	XP_016869211.1:p.Asp1367=
NM_001375654.1:c.787+5693G=	NP_001362583.1:n.787+5693G=
NM_006269.2:c.4099G= MANE Select	NP_006260.1:p.Asp1367=