Canonical Allele Identifier: CA1698611688

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096797G= , CM000669.2:g.33096797G=	GRCh38
NC_000007.13:g.33136409G= , CM000669.1:g.33136409G=	GRCh37
NC_000007.12:g.33102934G=	NCBI36
NG_012968.1:g.17594C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-243C=
ENST00000492391.2:n.1530-243C=
ENST00000682645.1:n.3477-243C=
ENST00000683432.1:c.*581-243C=	ENSP00000508174.1:n.*581-243C=
ENST00000684207.1:c.406-243C=	ENSP00000506942.1:n.406-243C=
ENST00000297157.8:c.406-243C= MANE Select	ENSP00000297157.3:n.406-243C=
ENST00000297157.7:c.406-243C=	ENSP00000297157.3:n.406-243C=
ENST00000448915.1:c.304-243C=	ENSP00000411577.1:n.304-243C=
NM_203288.1:c.406-243C=	NP_976033.1:n.406-243C=
XM_011515468.1:c.304-243C=	XP_011513770.1:n.304-243C=
XM_011515468.3:c.304-243C=	XP_011513770.1:n.304-243C=
NM_203288.2:c.406-243C= MANE Select	NP_976033.1:n.406-243C=