Canonical Allele Identifier: CA1785189089

Gene: RP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.54628213C= , CM000670.2:g.54628213C=	GRCh38
NC_000008.10:g.55540773C= , CM000670.1:g.55540773C=	GRCh37
NC_000008.9:g.55703326C=	NCBI36
NG_009840.1:g.17147C=
NG_009840.2:g.17147C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220676.2:c.4331C= MANE Select	ENSP00000220676.1:p.Thr1444=
ENST00000636932.1:c.787+5925C=	ENSP00000489857.1:n.787+5925C=
ENST00000637698.1:c.787+5925C=	ENSP00000490104.1:n.787+5925C=
ENST00000220676.1:c.4331C=	ENSP00000220676.1:p.Thr1444=
NM_006269.1:c.4331C=	NP_006260.1:p.Thr1444=
XM_017013721.1:c.4352C=	XP_016869210.1:p.Thr1451=
XM_017013722.1:c.4331C=	XP_016869211.1:p.Thr1444=
NM_001375654.1:c.787+5925C=	NP_001362583.1:n.787+5925C=
NM_006269.2:c.4331C= MANE Select	NP_006260.1:p.Thr1444=