Canonical Allele Identifier: CA1785188973

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54627978G= , CM000670.2:g.54627978G=	GRCh38
NC_000008.10:g.55540538G= , CM000670.1:g.55540538G=	GRCh37
NC_000008.9:g.55703091G=	NCBI36
NG_009840.1:g.16912G=
NG_009840.2:g.16912G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220676.2:c.4096G= MANE Select	ENSP00000220676.1:p.Asp1366=
ENST00000636932.1:c.787+5690G=	ENSP00000489857.1:n.787+5690G=
ENST00000637698.1:c.787+5690G=	ENSP00000490104.1:n.787+5690G=
ENST00000220676.1:c.4096G=	ENSP00000220676.1:p.Asp1366=
NM_006269.1:c.4096G=	NP_006260.1:p.Asp1366=
XM_017013721.1:c.4117G=	XP_016869210.1:p.Asp1373=
XM_017013722.1:c.4096G=	XP_016869211.1:p.Asp1366=
NM_001375654.1:c.787+5690G=	NP_001362583.1:n.787+5690G=
NM_006269.2:c.4096G= MANE Select	NP_006260.1:p.Asp1366=