Canonical Allele Identifier: CA1698611676

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096764C= , CM000669.2:g.33096764C=	GRCh38
NC_000007.13:g.33136376C= , CM000669.1:g.33136376C=	GRCh37
NC_000007.12:g.33102901C=	NCBI36
NG_012968.1:g.17627G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-210G=
ENST00000492391.2:n.1530-210G=
ENST00000682645.1:n.3477-210G=
ENST00000683432.1:c.*581-210G=	ENSP00000508174.1:n.*581-210G=
ENST00000684207.1:c.406-210G=	ENSP00000506942.1:n.406-210G=
ENST00000297157.8:c.406-210G= MANE Select	ENSP00000297157.3:n.406-210G=
ENST00000297157.7:c.406-210G=	ENSP00000297157.3:n.406-210G=
ENST00000448915.1:c.304-210G=	ENSP00000411577.1:n.304-210G=
NM_203288.1:c.406-210G=	NP_976033.1:n.406-210G=
XM_011515468.1:c.304-210G=	XP_011513770.1:n.304-210G=
XM_011515468.3:c.304-210G=	XP_011513770.1:n.304-210G=
NM_203288.2:c.406-210G= MANE Select	NP_976033.1:n.406-210G=